Redefining oxidative stress.

Oxidative stress is usually outlined as an imbalance of pro-oxidants and antioxidants, which could be quantified in people because the redox state of plasma GSH/GSSG. Plasma GSH redox in people turns into oxidized with age, in response to oxidative stress (chemotherapy, smoking), and in frequent illnesses (kind 2 diabetes, heart problems).
Nevertheless, information additionally present that redox of plasma GSH/GSSG just isn’t equilibrated with the bigger plasma cysteine/cystine (Cys/CySS) pool, indicating that the “stability” of pro-oxidants and antioxidants can’t be outlined by a single entity. The most important mobile thiol/disulfide programs, together with GSH/GSSG, thioredoxin- 1 (-SH(2)/-SS-), and Cys/CySS, usually are not in redox equilibrium and reply in another way to chemical toxicants and physiologic stimuli.
Particular person signaling and management occasions happen by means of discrete redox pathways quite than by means of mechanisms which are immediately conscious of a world thiol/disulfide stability similar to that conceptualized within the frequent definition of oxidative stress.
Thus, from a mechanistic standpoint, oxidative stress could also be higher outlined as a disruption of redox signaling and management. Adoption of such a definition may redirect analysis to determine key perturbations of redox signaling and management and result in new therapies for oxidative stress-related illness processes.

Complete evaluation of kinase inhibitor selectivity.

We examined the interplay of 72 kinase inhibitors with 442 kinases protecting >80% of the human catalytic protein kinome. Our information present that, as a category, kind II inhibitors are extra selective than kind I inhibitors, however that there are vital exceptions to this development. The information additional illustrate that selective inhibitors have been developed towards the vast majority of kinases focused by the compounds examined.
Evaluation of the interplay patterns reveals a category of ‘group-selective’ inhibitors broadly lively towards a single subfamily of kinases, however selective outdoors that subfamily. The information set suggests compounds to make use of as instruments to check kinases for which no devoted inhibitors exist.
It additionally supplies a basis for additional exploring kinase inhibitor biology and toxicity, in addition to for finding out the structural foundation of the noticed interplay patterns. Our findings will assist to appreciate the direct enabling potential of genomics for drug growth and fundamental analysis about mobile signaling.

Omega-Three fatty acids and heart problems: results on danger components, molecular pathways, and scientific occasions.

We reviewed obtainable proof for cardiovascular results of n-Three polyunsaturated fatty acid (PUFA) consumption, specializing in lengthy chain (seafood) n-Three PUFA, together with their principal dietary sources, results on physiological danger components, potential molecular pathways and bioactive metabolites, results on particular scientific endpoints, and present dietary pointers.
Main dietary sources embrace fatty fish and different seafood. n-Three PUFA consumption lowers plasma triglycerides, resting coronary heart fee, and blood stress and may additionally enhance myocardial filling and effectivity, decrease irritation, and enhance vascular operate.
Experimental research exhibit direct anti-arrhythmic results, which have been difficult to doc in people. n-Three PUFA have an effect on a myriad of molecular pathways, together with alteration of bodily and chemical properties of mobile membranes, direct interplay with and modulation of membrane channels and proteins, regulation of gene expression through nuclear receptors and transcription components, modifications in eicosanoid profiles, and conversion of n-Three PUFA to bioactive metabolites.
In potential observational research and adequately powered randomized scientific trials, advantages of n-Three PUFA appear most constant for coronary coronary heart illness mortality and sudden cardiac loss of life. Potential results on different cardiovascular outcomes are less-well-established, together with conflicting proof from observational research and/or randomized trials for results on nonfatal myocardial infarction, ischemic stroke, atrial fibrillation, recurrent ventricular arrhythmias, and coronary heart failure.
 Analysis gaps embrace the relative significance of various physiological and molecular mechanisms, exact dose-responses of physiological and scientific results, whether or not fish oil supplies all the advantages of fish consumption, and scientific results of plant-derived n-Three PUFA.
Total, present information present sturdy concordant proof that n-Three PUFA are bioactive compounds that cut back danger of cardiac loss of life. Nationwide and worldwide pointers have converged on constant suggestions for the final inhabitants to devour no less than 250 mg/day of long-chain n-Three PUFA or no less than 2 servings/week of oily fish.

A circuitry mannequin of the expression of behavioral sensitization to amphetamine-like psychostimulants.

Repeated publicity to psychostimulants similar to cocaine and amphetamine produces behavioral sensitization, which is characterised by an augmented locomotor response to a subsequent psychostimulant problem injection. Experimentation centered on the neural underpinnings of behavioral sensitization has progressed from a singular concentrate on dopamine transmission within the nucleus accumbens and striatum to the research of mobile and molecular mechanisms that happen all through the neural circuitry wherein the mesocorticolimbic dopamine projections are embedded.
This analysis effort has yielded a conglomerate of information that has resisted easy interpretations, primarily as a result of no single neuronal impact is prone to be accountable for the expression of behavioral sensitization. The current evaluation examines the literature and critically evaluates the extent to which the neural penalties of repeated psychostimulant administration are related to the expression of behavioral sensitization.
The neural alterations discovered to contribute to the long-term expression of behavioral sensitization are centered in a set of interconnected limbic nuclei, that are termed the ‘motive’ circuit. This neural circuit is used as a template to arrange the related biochemical and molecular findings right into a mannequin of the expression of behavioral sensitization.

Oxidative stress as a significant wrongdoer in kidney illness in diabetes.

It’s postulated that localized tissue oxidative stress is a key element within the growth of diabetic nephropathy. There stays controversy, nonetheless, as as to whether that is an early hyperlink between hyperglycemia and renal illness or develops as a consequence of different major pathogenic mechanisms.
Within the kidney, a variety of pathways that generate reactive oxygen species (ROS) similar to glycolysis, particular defects within the polyol pathway, uncoupling of nitric oxide synthase, xanthine oxidase, NAD(P)H oxidase, and superior glycation have been recognized as doubtlessly main contributors to the pathogenesis of diabetic kidney illness.
As well as, a unifying speculation has been proposed whereby mitochondrial manufacturing of ROS in response to persistent hyperglycemia often is the key initiator for every of those pathogenic pathways. This postulate emphasizes the significance of mitochondrial dysfunction within the development and growth of diabetes issues together with nephropathy.
A thriller stays, nonetheless, as to why antioxidants per se have demonstrated minimal renoprotection in people regardless of constructive preclinical analysis findings. It’s doubtless that the utility of present research approaches, similar to vitamin use, will not be the perfect antioxidant technique in human diabetic nephropathy.

CFDA SE Cell Tracer Kit

K1023-1 1 kit
EUR 96
Description: The CFDA SE (carboxyfluorescein diacetate succinimidyl ester) Cell Tracer Kit is usually used in fluorescence analyses as a long-term tracer of cells. The Kit can be used for in vitro and in vivo labeling of cells to determine whether or not a cell is proliferating, especially.

FluoGreen Tracer

SF41000 100 ul
EUR 522

CFDA SE cell proliferation and tracer detection kit

ETF0051 2000 assays
EUR 300

Tau tracer 1

T39660-10mg 10mg Ask for price
Description: Tau tracer 1

Tau tracer 1

T39660-1g 1g Ask for price
Description: Tau tracer 1

Tau tracer 1

T39660-1mg 1mg Ask for price
Description: Tau tracer 1

Tau tracer 1

T39660-50mg 50mg Ask for price
Description: Tau tracer 1

Tau tracer 1

T39660-5mg 5mg Ask for price
Description: Tau tracer 1

Tau tracer 2

T37051-10mg 10mg Ask for price
Description: Tau tracer 2

Tau tracer 2

T37051-1g 1g Ask for price
Description: Tau tracer 2

Tau tracer 2

T37051-1mg 1mg Ask for price
Description: Tau tracer 2

Tau tracer 2

T37051-50mg 50mg Ask for price
Description: Tau tracer 2

Tau tracer 2

T37051-5mg 5mg Ask for price
Description: Tau tracer 2

JAK2 JH2 Tracer

HY-102055 50mg
EUR 5515.2

JAK2 JH2 Tracer

T19017-10mg 10mg Ask for price
Description: JAK2 JH2 Tracer

JAK2 JH2 Tracer

T19017-1g 1g Ask for price
Description: JAK2 JH2 Tracer

JAK2 JH2 Tracer

T19017-1mg 1mg Ask for price
Description: JAK2 JH2 Tracer

JAK2 JH2 Tracer

T19017-50mg 50mg Ask for price
Description: JAK2 JH2 Tracer

JAK2 JH2 Tracer

T19017-5mg 5mg Ask for price
Description: JAK2 JH2 Tracer

CytoFixâ„¢ BCECF, AM *Optimized for long term cellular pH tracking*

21200-1mg 1 mg
EUR 318
Description: Intracellular pH plays an important modulating role in many cellular events, including cell growth, calcium regulation, enzymatic activity, receptor-mediated signal transduction, ion transport, endocytosis, chemotaxis, cell adhesion and other cellular processes.

ROS tracer precursor

T19550-10mg 10mg Ask for price
Description: ROS tracer precursor

ROS tracer precursor

T19550-1g 1g Ask for price
Description: ROS tracer precursor

ROS tracer precursor

T19550-1mg 1mg Ask for price
Description: ROS tracer precursor

ROS tracer precursor

T19550-50mg 50mg Ask for price
Description: ROS tracer precursor

ROS tracer precursor

T19550-5mg 5mg Ask for price
Description: ROS tracer precursor

Long-Term Cell Tracing Reagent CMAC (Blue)

EGY0171 100µg
EUR 92

Long-Term Cell Tracing Reagent CMAC (Blue)

EGY0172 5x100µg
EUR 340

Long-Term Cell Tracing Reagent CMFDA(Green)

EGY0181 100µg
EUR 220

Long-Term Cell Tracing Reagent CMFDA(Green)

EGY0182 5x100µg
EUR 500

Long-Term Cell Tracing Reagent CDCFDA, SE (Green)

EGY0161 100 µg
EUR 160

Long-Term Cell Tracing Reagent CDCFDA, SE (Green)

EGY0162 5 x 100 µg
EUR 340

NIR-FLIVO® 690 Tracer In vivo Assay

9112 20 Tests
EUR 438

NIR-FLIVO® 747 Tracer In vivo Assay

9114 20 Tests
EUR 438

CytoSelect™ Cell Transformation Assay (Cell Recovery Compatible), Colorimetric

CBA-135 96 assays
EUR 715

CytoSelect™ Cell Transformation Assay (Cell Recovery Compatible), Colorimetric

CBA-135-5 5 x 96 assays
EUR 3095

CytoSelect™ Cell Transformation Assay (Cell Recovery Compatible), Fluorometric

CBA-140 96 assays
EUR 750

CytoSelect™ Cell Transformation Assay (Cell Recovery Compatible), Fluorometric

CBA-140-5 5 x 96 assays
EUR 3215

CytoSelect Cell Transformation Assay (Cell Recovery Compatible), Colorimetric, Trial Size

CBA-135-T 24 assays
EUR 518.4
Description: CytoSelect 96-Well Cell Transformation Assays (Cell Recovery Compatible) provide a robust system for detecting transformed cells, screening cell transformation inhibitors, and determining in vitro drug sensitivity. A proprietary modified soft agar matrix allows you to either quantify cells using the included fluorescent dye, or recover the cells for further analysis.

CytoSelect 96-Well Cell Transformation Assay (Cell Recovery Compatible, Fluorometric), Trial Size

CBA-140-T 24 assays
EUR 547.2
Description: CytoSelect 96-Well Cell Transformation Assays (Cell Recovery Compatible) provide a robust system for detecting transformed cells, screening cell transformation inhibitors, and determining in vitro drug sensitivity. A proprietary modified soft agar matrix allows you to either quantify cells using the included fluorescent dye, or recover the cells for further analysis.

CytoSelect™ 96-well Cell Transformation Assay

CBA-130 96 assays
EUR 640

CytoSelect™ 96-well Cell Transformation Assay

CBA-130-5 5 x 96 assays
EUR 2695

CytoSelect 384-well Cell Transformation Assay, Fluorometric

CBA-145 384 assays
EUR 1208.4
Description: Our CytoSelect 384-Well Cell Transformation Assay uses a modified soft agar 3D matrix to support the formation of colonies by neoplastic cells. Quantitation of cell transformation is performed on a fluorescence plate reader.

CytoSelect 384-well Cell Transformation Assay, Fluorometric

CBA-145-5 5 x 384 assays
EUR 4681.2
Description: Our CytoSelect 384-Well Cell Transformation Assay uses a modified soft agar 3D matrix to support the formation of colonies by neoplastic cells. Quantitation of cell transformation is performed on a fluorescence plate reader.

293AD Cell Line

AD-100 1 vial
EUR 365

293AAV Cell Line

AAV-100 1 vial
EUR 405

293LTV Cell Line

LTV-100 1 vial
EUR 405

293RTV Cell Line

RV-100 1 vial
EUR 405

StemTAG Stem Cell Colony Formation Assay (Cell Recovery Compatible)

CBA-325 96 assays
EUR 1027.2
Description: Our StemTAG 96-Well Stem Cell Colony Formation Assay provides a high-throughput method to quantify ES cells in just 7-10 days, and no manual cell counting is required. Once colonies are formed, they may be analyzed in three different ways: 1. Lyse cells, then quantify in a fluorescence plate reader using dye included in the kit; 2. Lyse cells, then quantify alkaline phosphatase activity using reagents provided; or 3. Recover colonies from matrix for further culture or analysis.

StemTAG Stem Cell Colony Formation Assay (Cell Recovery Compatible)

CBA-325-5 5 x 96 assays
EUR 4033.2
Description: Our StemTAG 96-Well Stem Cell Colony Formation Assay provides a high-throughput method to quantify ES cells in just 7-10 days, and no manual cell counting is required. Once colonies are formed, they may be analyzed in three different ways: 1. Lyse cells, then quantify in a fluorescence plate reader using dye included in the kit; 2. Lyse cells, then quantify alkaline phosphatase activity using reagents provided; or 3. Recover colonies from matrix for further culture or analysis.

293/GFP Cell Line

AKR-200 1 vial
EUR 460

T47D/GFP Cell Line

AKR-208 1 vial
EUR 686.4
Description: T47D/GFP Cell Line stably expresses GFP and otherwise exhibits the same characteristics of the parental cell line.

A549/GFP Cell Line

AKR-209 1 vial
EUR 460

HeLa/GFP Cell Line

AKR-213 1 vial
EUR 460

293/Cas9 Cell Line

AKR-5110 1 vial
EUR 460

HeLa/Cas9 Cell Line

AKR-5111 1 vial
EUR 460

NIH3T3/GFP Cell Line

AKR-214 1 vial
EUR 460

NIH3T3/Cas9 Cell Line

AKR-5104 1 vial
EUR 460

MCF-7/Luc Cell Line

AKR-234 1 vial
EUR 686.4
Description: MCF-7/Luc Cell Line stably expresses luciferase and otherwise exhibits the same characteristics of the parental cell line.

SKOV-3/Luc Cell Line

AKR-232 1 vial
EUR 686.4
Description: SKOV-3/Luc Cell Line stably expresses luciferase and otherwise exhibits the same characteristics of the parental cell line.

OVCAR-5/RFP Cell Line

AKR-254 1 vial
EUR 686.4
Description: OVCAR-5/RFP Cell Line stably expresses RFP and otherwise exhibits the same characteristics of the parental cell line.

CytoSelect™ 96-Well Cell Transformation Assay (Soft Agar Colony Formation), Trial Size

CBA-130-T 24 assays
EUR 320

Collagen-based Cell Contraction Assay

CBA-201 24 assays
EUR 420

Radius 384-Well Cell Migration Assay

CBA-127 384 assays
EUR 721.2
Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap.

Radius 384-Well Cell Migration Assay

CBA-127-5 5 x 384 wells
EUR 2802
Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap.

HIF-1 Alpha Cell Based ELISA Kit

CBA-281 96 assays
EUR 734.4
Description: Cell Biolabs? HIF-1 Cell Based ELISA Kit is an immunoassay developed for rapid detection of HIF-1 Alpha in fixed cells. Cells on a microplate are stimulated for HIF-1 Alpha stabilization, fixed, permeabilized, and then neutralized in the well. HIF-1 Alpha is then detected with an anti-HIF-1 alpha antibody followed by an HRP conjugated secondary antibody. Each kit provides sufficient reagents to perform up to a total of 96 assays and can detect HIF-1 Alpha from human, mouse, or rat.

CytoSelect™ MTT Cell Proliferation Assay

CBA-252 960 assays
EUR 320

Radius™ 24-Well Cell Migration Assay

CBA-125 24 assays
EUR 425

Radius™ 24-Well Cell Migration Assay

CBA-125-5 5 x 24 assays
EUR 1820

Radius™ 96-Well Cell Migration Assay

CBA-126 96 assays
EUR 495

Radius™ 96-Well Cell Migration Assay

CBA-126-5 5 x 96 assays
EUR 2095

Radius™ 48-Well Cell Migration Assay

CBA-5037 48 assays
EUR 445

Radius™ 48-Well Cell Migration Assay

CBA-5037-5 5 x 48 assays
EUR 1895

CytoSelect™ BrdU Cell Proliferation ELISA Kit

CBA-251 96 assays
EUR 455

CytoSelect Cell Proliferation Assay Reagent (Fluorometric)

CBA-250 10 mL
EUR 490.8
Description: Cell Biolabs? CytoSelect Cell Proliferation Assay Reagent (Fluorometric) provides a fluorometric format for measuring and monitoring cell proliferation. Cells can be plated and then treated with compounds or agents that affect proliferation.  Cells are then incubated with the proliferation reagent.  Upon entering metabolically active live cells, the non-fluorescent proliferation reagent is converted into a bright red fluorescent form. An increase in cell proliferation is accompanied by increased fluorescent signal, while a decrease in cell proliferation (and signal) can indicate the toxic effects of compounds or suboptimal culture conditions.  The assay principles are basic and can be applied to most eukaryotic cell lines, including adherent and non-adherent cells and certain tissues.  This cell proliferation reagent can be used to detect proliferation in bacteria, yeast, fungi, protozoa as well as cultured mammalian and piscine cells. The kit contains sufficient reagents for the evaluation of 960 assays in ten 96-well plates or 192 assays in eight 24-well plates.

CytoSelect™ Cell Viability and Cytotoxicity Assay

CBA-240 96 assays
EUR 305

Platinum-E Retroviral Packaging Cell Line, Ecotropic

RV-101 1 vial
EUR 770

Platinum-GP Retroviral Packaging Cell Line, Pantropic

RV-103 1 vial
EUR 770

CytoSelect™ 24-Well Cell Co-Culture System

CBA-160 24 assays
EUR 365

CytoSelect™ 24-Well Cell Co-Culture System

CBA-160-5 5 x 24 assays
EUR 1585

Total Protein - Murine Embryonic Stem Cell Line D3

CBA-305 500 ?g
EUR 414
Description:
  • Isolated from mouse ES-D3 cell line
  • Presented as 500 µg at 1 mg/mL in NP-40 Solubilization Buffer

CytoSelect 24-well Laminin Cell Invasion, Colorimetric

CBA-110-LN 12 assays
EUR 714
Description: The ability of malignant tumor cells to invade normal surrounding tissue contributes in large part to the morbidity and mortality of cancers. Cell invasion requires several distinct cellular functions including adhesion, motility, detachment, and extracellular matrix proteolysis. Our CytoSelect Cell Invasion Assays utilize precoated inserts to assay the invasive properties of tumor cells. Invasive cells can be quantified in 24-well plates on either a standard microplate reader or a fluorescence plate reader. Inserts are precoated on the top of the membrane with Laminin.

Platinum-A Retroviral Packaging Cell Line, Amphotropic

RV-102 1 vial
EUR 770

CytoSelect™ 48-Well Cell Contraction Assay Kit

CBA-5021 48 assays
EUR 575

CytoSelect™ Cell Proliferation Assay Reagent (Colorimetric)

CBA-253 10 mL
EUR 320

Radius 24-Well Cell Migration Assay, (Laminin Coated)

CBA-125-LN 24 assays
EUR 714
Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap.

StemTAG PCR Primer Set for Stem Cell Characterization

CBA-303 1 kit
EUR 470.4
Description: StemTAG PCR Primer Set for Stem Cell Characterization includes 7 primer pairs: Oct-4, NANOG, AFP, Flk-1, and NCAM, plus GAPDH and beta-actin as controls.

CytoSelect Clonogenic Tumor Cell Isolation Kit (5 preps)

CBA-155 5 preps
EUR 957.6
Description: Many solid tumors contain heterogeneous populations of normal and cancerous cells. Separation of these cell populations is key to an accurate assessment of the true genotypic and phenotypic differences between normal and tumor cells. Our CytoSelect Clonogenic Tumor Cell Isolation Kit uses a proprietary semisolid agar medium to facilitate formation of colonies by cells from solid tumors. Colonies are grown in either a 6-well plate or a 35mm culture dish. These colonies are isolated away from single (i.e. normal) cells by size filtration. The viable cells from these colonies can be easily recovered for further analysis.

Radius 24-Well Cell Migration Assay, (Fibronectin Coated)

CBA-125-FN 24 assays
EUR 714
Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap.

CytoSelect™ 24-well Collagen Cell Invasion, Colorimetric

CBA-110-COL 12 assays
EUR 535

Radius 24-Well Cell Migration Assay, (ECM Array Coated)

CBA-125-ECM 24 wells
EUR 838.8
Description: The Radius Cell Migration Assay provides a unique alternative to conventional cell migration assays using the Boyden chamber. Unlike Boyden chamber assays which may only be analyzed at endpoint, the Radius assay uses a proprietary cell culture plate containing a carefully-defined biocompatible hydrogel (Radius gel) spot centralized at the bottom of each well. When cells are seeded in the well, they will attach everywhere except on the Radius gel, creating a cell-free zone. Following cell seeding the Radius gel is removed, allowing migratory cells to move across the area and close the gap.

CytoSelect Proliferating Cell Nuclear Antigen (PCNA) ELISA Kit

CBA-254 96 assays
EUR 672
Description: Cell Biolabs? CytoSelect Proliferating Cell Nuclear Antigen (PCNA) ELISA Kit is an enzyme immunoassay developed for the detection and quantitation of PCNA from nuclear and whole cell extracts.  The kit detects PCNA from mouse, rat and human, and has a detection sensitivity limit of 12.5 ng/mLPCNA.  Each kit provides sufficient reagents to perform up to 96 assays including standard curve and unknown samples. 

CytoSelect 48-well Cell Adhesion Assay (Laminin, Colorimetric)

CBA-056 48 assays
EUR 512.4
Description: Cell adhesion is a complex process involved in migration/invasion, embryogenesis, wound healing and tissue remodeling. Cells adhere to the extracellular matrix, forming complexes with cytoskeleton components that can affect cell motility, differentiation, proliferation, and survival. Our CytoSelect 48-Well Cell Adhesion Assays provide a fully quantitative method for the evaluation of cell adhesion. The 48-well plate is precoated with Laminin.

CytoSelect 48-well Cell Adhesion Assay (Laminin, Fluorometric)

CBA-057 48 assays
EUR 553.2
Description: Cell adhesion is a complex process involved in migration/invasion, embryogenesis, wound healing and tissue remodeling. Cells adhere to the extracellular matrix, forming complexes with cytoskeleton components that can affect cell motility, differentiation, proliferation, and survival. Our CytoSelect 48-Well Cell Adhesion Assays provide a fully quantitative method for the evaluation of cell adhesion. The 48-well plate is precoated with Laminin.

CytoSelect 24-well Laminin Cell Invasion Assay, Fluorometric

CBA-111-LN 12 assays
EUR 714
Description: The ability of malignant tumor cells to invade normal surrounding tissue contributes in large part to the morbidity and mortality of cancers. Cell invasion requires several distinct cellular functions including adhesion, motility, detachment, and extracellular matrix proteolysis. Our CytoSelect Cell Invasion Assays utilize precoated inserts to assay the invasive properties of tumor cells. Invasive cells can be quantified in 24-well plates on either a standard microplate reader or a fluorescence plate reader. Inserts are precoated on the top of the membrane with Laminin.

CytoSelect 96-well Laminin Cell Invasion Assay, Fluorometric

CBA-112-LN 96 assays
EUR 908.4
Description: The ability of malignant tumor cells to invade normal surrounding tissue contributes in large part to the morbidity and mortality of cancers. Cell invasion requires several distinct cellular functions including adhesion, motility, detachment, and extracellular matrix proteolysis. Our CytoSelect 96-Well Cell Invasion Assays utilize precoated inserts to assay the invasive properties of tumor cells. Invasive cells can be quantified in 96-well plates on a fluorescence plate reader. Inserts are precoated on the top of the membrane with Laminin.

CytoSelect 48-well Cell Adhesion Assay (Fibrinogen, Colorimetric)

CBA-058 48 assays
EUR 512.4
Description: Cell adhesion is a complex process involved in migration/invasion, embryogenesis, wound healing and tissue remodeling. Cells adhere to the extracellular matrix, forming complexes with cytoskeleton components that can affect cell motility, differentiation, proliferation, and survival. Our CytoSelect 48-Well Cell Adhesion Assays provide a fully quantitative method for the evaluation of cell adhesion. The 48-well plate is precoated with Fibrinogen.

CytoSelect 48-well Cell Adhesion Assay (Fibrinogen, Fluorometric)

CBA-059 48 assays
EUR 553.2
Description: Cell adhesion is a complex process involved in migration/invasion, embryogenesis, wound healing and tissue remodeling. Cells adhere to the extracellular matrix, forming complexes with cytoskeleton components that can affect cell motility, differentiation, proliferation, and survival. Our CytoSelect 48-Well Cell Adhesion Assays provide a fully quantitative method for the evaluation of cell adhesion. The 48-well plate is precoated with Fibrinogen.

CytoSelect™ 96-well Phagocytosis Assay (Red Blood Cell)

CBA-220 96 assays
EUR 540

Radius™ 24-Well Cell Migration Assay, (Collagen I Coated)

CBA-125-COL 24 assays
EUR 520

CytoSelect™ 24-well Collagen Cell Invasion Assay, Fluorometric

CBA-111-COL 12 assays
EUR 535

CytoSelect™ 96-well Collagen Cell Invasion Assay, Fluorometric

CBA-112-COL 96 assays
EUR 705

CytoSelect Clonogenic Tumor Cell Isolation Kit (5 x 5 preps)

CBA-155-5 25 preps
EUR 3894
Description: Many solid tumors contain heterogeneous populations of normal and cancerous cells. Separation of these cell populations is key to an accurate assessment of the true genotypic and phenotypic differences between normal and tumor cells. Our CytoSelect Clonogenic Tumor Cell Isolation Kit uses a proprietary semisolid agar medium to facilitate formation of colonies by cells from solid tumors. Colonies are grown in either a 6-well plate or a 35mm culture dish. These colonies are isolated away from single (i.e. normal) cells by size filtration. The viable cells from these colonies can be easily recovered for further analysis.

CytoSelect™ 48-well Cell Adhesion Assay (Fibronectin, Colorimetric)

CBA-050 48 assays
EUR 370

CytoSelect™ 48-well Cell Adhesion Assay (Fibronectin, Fluorometric)

CBA-051 48 assays
EUR 400

CytoSelect™ 24-well Cell Invasion (Basement Membrane), Fluorometric

CBA-111 12 assays
EUR 535

CytoSelect™ 24-well Cell Migration Assay (8 μm), Colorimetric

CBA-100 12 assays
EUR 480

CytoSelect™ 24-well Cell Migration Assay (8 μm), Colorimetric

CBA-100-5 5 x 12 assays
EUR 2180

CytoSelect™ 24-well Cell Migration Assay (8 μm), Fluorometric

CBA-101 12 assays
EUR 480

CytoSelect™ 24-well Cell Migration Assay (8 μm), Fluorometric

CBA-101-5 5 x 12 assays
EUR 2180

CytoSelect™ 24-well Cell Migration Assay (5 μm), Fluorometric

CBA-102 12 assays
EUR 480

CytoSelect™ 24-well Cell Migration Assay (5 μm), Fluorometric

CBA-102-5 5 x 12 assays
EUR 2180

CytoSelect™ 24-well Cell Migration Assay (3 μm), Fluorometric

CBA-103 12 assays
EUR 480

CytoSelect™ 24-well Cell Migration Assay (3 μm), Fluorometric

CBA-103-5 5 x 12 assays
EUR 2180

CytoSelect™ 96-well Cell Migration Assay (3 μm), Fluorometric

CBA-104 96 assays
EUR 580

CytoSelect™ 96-well Cell Migration Assay (3 μm), Fluorometric

CBA-104-5 5 x 96 assays
EUR 2535

CytoSelect™ 96-well Cell Migration Assay (5 μm), Fluorometric

CBA-105 96 assays
EUR 580

CytoSelect™ 96-well Cell Migration Assay (5 μm), Fluorometric

CBA-105-5 5 x 96 assays
EUR 2535

CytoSelect™ 96-well Cell Migration Assay (8 μm), Fluorometric

CBA-106 96 assays
EUR 580

CytoSelect™ 96-well Cell Migration Assay (8 μm), Fluorometric

CBA-106-5 5 x 96 assays
EUR 2535

CytoSelect™ 24-well Cell Migration Assay (12 μm), Colorimetric

CBA-107 12 assays
EUR 480

CytoSelect™ 24-well Cell Migration Assay (12 μm), Fluorometric

CBA-108 12 assays
EUR 480

CytoSelect™ 48-well Cell Adhesion Assay (ECM Array, Colorimetric)

CBA-070 48 assays
EUR 515

CytoSelect™ 48-well Cell Adhesion Assay (ECM Array, Colorimetric)

CBA-070-5 5 x 48 assays
EUR 2275

CytoSelect™ 48-well Cell Adhesion Assay (ECM Array, Fluorometric)

CBA-071 48 assays
EUR 555

CytoSelect™ 48-well Cell Adhesion Assay (ECM Array, Fluorometric)

CBA-071-5 5 x 48 assays
EUR 2430

CytoSelect™ 48-well Cell Adhesion Assay (Collagen I, Colorimetric)

CBA-052 48 assays
EUR 370

CytoSelect™ 48-well Cell Adhesion Assay (Collagen I, Fluorometric)

CBA-053 48 assays
EUR 400

CytoSelect™ 48-well Cell Adhesion Assay (Collagen IV, Colorimetric)

CBA-060 48 assays
EUR 370

CytoSelect™ 48-well Cell Adhesion Assay (Collagen IV, Fluorometric)

CBA-061 48 assays
EUR 400

CytoSelect™ 24-well Cell Invasion Assay (Basement Membrane), Colorimetric

CBA-110 12 assays
EUR 535

CytoSelect™ 96-well Cell Invasion Assay (Basement Membrane), Fluorometric

CBA-112 96 assays
EUR 705

CytoSelect™ 96-Well Hematopoietic Colony Forming Cell Assay (96 assays)

CBA-320 96 assays
EUR 440

CytoSelect™ 24-Well Cell Contraction Assay Kit (Floating Matrix Model)

CBA-5020 24 assays
EUR 495

CytoSelect™ 24-well Cell Haptotaxis Assay (8 µm), FN-coated, Colorimetric

CBA-100-FN 12 assays
EUR 505

CytoSelect™ 24-well Cell Haptotaxis Assay (8 µm), FN-coated, Fluorometric

CBA-101-FN 12 assays
EUR 505

CytoSelect™ 24-well Cell Haptotaxis Assay (8 µm), COL-coated, Colorimetric

CBA-100-COL 12 assays
EUR 505

CytoSelect™ 24-well Cell Haptotaxis Assay (8 µm), COL-coated, Fluorometric

CBA-101-COL 12 assays
EUR 505
There may be now an growing physique of information to counsel that methods involving a extra focused antioxidant method, utilizing brokers that penetrate particular mobile compartments, often is the elusive additive remedy required to additional optimize renoprotection in diabetes.

Leave a Comment