추천 제품
제조업체/상표
Chemicon®
QCM
Quality Level
기술
cell based assay: suitable
검출 방법
colorimetric
fluorometric
배송 상태
wet ice
일반 설명
Also available: Cell Comb Scratch Assay! Get biochemical data from a scratch assay!Click Here
Introduction
Angiogenesis is a fundamental process involving the growth of new blood vessels from pre-existing vessels. It is important in development and wound healing, as well as pathologic diseases such as diabetic retinopathy and cancer. During angiogenesis, endothelial cells need to move out of existing vessels, migrate into new areas, proliferate and assemble into new capillaries. The migration of endothelial cells is regulated by many angiogenic factors and anti-angiogenic factors. It is critical for researchers to understand the mechanisms of endothelial cell migration.
Millipore′s 3 μm QCM Endothelial Cell Migration Assay – Fibronectin, Colorimetric provides a quick and efficient system to study the ability of compounds to induce or inhibit endothelial cell migration. This assay also allows screening of pharmacological agents, evaluation of integrins or other adhesion receptors responsible for endothelial cell migration, analysis of gene function in transfected cells, and determination of ECM protein involvement in cell movement.
This versatile assay permits counting of individual migratory cells, and, more importantly, allows quantitative analysis by optical density (OD) using a standard microplate reader. This convenient assay allows large scale screening and quantitative comparison of multiple samples and includes individual migration controls for each sample.
Introduction
Angiogenesis is a fundamental process involving the growth of new blood vessels from pre-existing vessels. It is important in development and wound healing, as well as pathologic diseases such as diabetic retinopathy and cancer. During angiogenesis, endothelial cells need to move out of existing vessels, migrate into new areas, proliferate and assemble into new capillaries. The migration of endothelial cells is regulated by many angiogenic factors and anti-angiogenic factors. It is critical for researchers to understand the mechanisms of endothelial cell migration.
Millipore′s 3 μm QCM Endothelial Cell Migration Assay – Fibronectin, Colorimetric provides a quick and efficient system to study the ability of compounds to induce or inhibit endothelial cell migration. This assay also allows screening of pharmacological agents, evaluation of integrins or other adhesion receptors responsible for endothelial cell migration, analysis of gene function in transfected cells, and determination of ECM protein involvement in cell movement.
This versatile assay permits counting of individual migratory cells, and, more importantly, allows quantitative analysis by optical density (OD) using a standard microplate reader. This convenient assay allows large scale screening and quantitative comparison of multiple samples and includes individual migration controls for each sample.
애플리케이션
The Millipore QCM 3 μm Endothelial Cell Migration Assay – Fibronectin, Colorimetric is ideal for the study of endothelial cell migration in response to an angiogenic stimulus. The quantitative nature of this assay is especially useful for large scale screening of pharmacologic agents. BSA-coated control chambers provide an appropriate migration control. The 3 μm pore size in this assay is optimal for endothelial cells such as HUVEC, but not sufficient for fibroblast migration. The Millipore QCM 3 μm Endothelial Cell Migration Assay – Fibronectin, Colorimetric assay is intended for research use only; not for diagnostic applications.
Each kit provides sufficient materials for the evaluation of 12 samples.
Each kit provides sufficient materials for the evaluation of 12 samples.
포장
Sufficient for 12 assays
성분
1. Fibronectin Test Plate: One 24-well culture plate, containing 12 human FN-coated Boyden chambers, sufficient for the evaluation of 12 test samples.
2. BSA Control Plate: One 24-well culture plate, containing 12 BSA-coated Boyden chambers, sufficient for the evaluation of 12 controls.
3. Cell Stain Solution: One vial - 10 mL
4. Extraction Buffer: One vial - 10 mL
5. 24-Well Stain Extraction Plate
6. 96-Well Stain Quantitation Plate
7. Swabs: 50 ea
8. Forceps: 1 pair
2. BSA Control Plate: One 24-well culture plate, containing 12 BSA-coated Boyden chambers, sufficient for the evaluation of 12 controls.
3. Cell Stain Solution: One vial - 10 mL
4. Extraction Buffer: One vial - 10 mL
5. 24-Well Stain Extraction Plate
6. 96-Well Stain Quantitation Plate
7. Swabs: 50 ea
8. Forceps: 1 pair
저장 및 안정성
Store kit materials at 2° to 8°C for up to their expiration date. Do not freeze.
법적 정보
Accutase is a registered trademark of Innovative Cell Technologies, Inc.
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
면책조항
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Positive influence of AP-2alpha transcription factor on cadherin gene expression and differentiation of the ocular surface.
Judith A West-Mays, Jeremy M Sivak, Steve S Papagiotas, Jennifer Kim, Timothy Nottoli et al.
Differentiation null
Bingchen Han et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 30(2), 672-687 (2021-07-19)
Triple-negative breast cancer (TNBC) has a high propensity for organ-specific metastasis. However, the underlying mechanisms are not well understood. Here we show that the primary TNBC tumor-derived C-X-C motif chemokines 1/2/8 (CXCL1/2/8) stimulate lung-resident fibroblasts to produce the C-C motif
Maximilian Seles et al.
Cancers, 12(5) (2020-05-14)
POU3F3 adjacent non-coding transcript 1 (PANTR1) is an oncogenic long non-coding RNA with significant influence on numerous cellular features in different types of cancer. No characterization of its role in renal cell carcinoma (RCC) is yet available. In this study
문서
Cell based angiogenesis assays to analyze new blood vessel formation for applications of cancer research, tissue regeneration and vascular biology.
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