Selecione um tamanho
Sobre este item
Pular para
fabricante/nome comercial
Cell Comb™
Chemicon®
QCM
Nível de qualidade
técnica(s)
activity assay: suitable
cell based assay: suitable
western blot: suitable
Condições de expedição
ambient
1 of 4
Este Item | ECM510 | ECM210 | ECM555 |
|---|---|---|---|
| technique(s) activity assay: suitable, western blot: suitable, cell based assay: suitable | technique(s) activity assay: suitable, cell based assay: suitable | technique(s) cell based assay: suitable | technique(s) activity assay: suitable, cell based assay: suitable |
| manufacturer/tradename Cell Comb™, QCM, Chemicon® | manufacturer/tradename Chemicon®, QCM | manufacturer/tradename Chemicon®, QCM | manufacturer/tradename Chemicon®, QCM |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| shipped in ambient | shipped in wet ice | shipped in wet ice | shipped in wet ice |
Descrição geral
Click Here!
Cell migration can be studied by a variety of methods, but the scratch assay remains a highly popular method due to the simplicity of the required materials, experimental setup, data collection and interpretation (Lian, C., et al., 2007; Cory, G., 2011). The scratch assay is typically initiated by scratching a confluent cell monolayer with a pipette tip to create a narrow wound-like gap. Shortly after wounding, the cells at the edge of the wound initiate a program to migrate into the gap, a process that continues until the gap has been completely repopulated with cells. Extent of wound closure is typically observed through light microscopy and protein expression patterns that occur during the wound healing process can be characterized by immunofluorescence.
Advances in understanding the repair mechanisms of wounded cell monolayers have been facilitated by the development of methods for performing the assay in multiwell plates. Such methods include delivering wounds to existing monolayers in the wells, or occlusion of the center of the well during monolayer formation to create a gap (Yarrow, J.C., et al., 2004; Simpson K.J., et al., 2008; Gough, W., et al., 2011). Each method then involves quantification of the extent of cell migration into the gap.
However, these methods are not optimal for biochemical analysis of the molecular events mediating wound repair. For example, the small scale of a basic pipette tip-derived wound provides insufficient and inadequate material for biochemical analysis. Using the same pipette tip to scratch a cell monolayer in a larger plate is tedious and irreproducible, and the proportion of migrating cells to quiescent cells is low. Several methods have been described to scale up the scratch assay by creating multiple wounds in cell monolayers but these methods require specialized tools (Turchi, L., et al., 2002; Lauder, H., et al., 1998).
EMD Millipore has developed the Cell Comb™ Scratch Assay to address the need for an easy-to-use tool for creating multiple scratch wounds. The patent pending Cell Comb<TMSYMBOL></TMSYMBOL> has been optimized to apply a high density field of scratches to maximize the area of wound edges, while leaving sufficient numbers of undamaged cells to migrate into the gap. This form of high density wounding creates a high proportion of migrating cells to quiescent monolayer cells, which permits sensitive detection of the biochemical events occurring, specifically in the migrating cell population.
Aplicação
Cell Structure
Embalagem
Nota de preparo
Outras notas
Rectangular Cell Culture Plates: Quantity of 6 individually packaged, cell culture-treated 86 mm x 128 mm plates.
The Cell Combs and Cell Culture Plates have been subjected to E-beam irradiation in order to minimize the possibility of contamination.
Informações legais
Exoneração de responsabilidade
Código de classe de armazenamento
10 - Combustible liquids
Certificados de análise (COA)
Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.
Já possui este produto?
Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
Artigos
Cell based angiogenesis assays to analyze new blood vessel formation for applications of cancer research, tissue regeneration and vascular biology.
Conteúdo relacionado
"The successful, reliable culture of epithelial cells is critical for many areas of research, including dermatology, respiratory research, and cancer research. Because the breakdown of control mechanisms in epithelial cells is a frequent contributor to cancer progression and metastasis, epithelial cell culture is particularly important for cancer research. EpiGRO™ media formulations are optimized to provide better viability, proliferation rates, morphology and culture stability than other commercially available options. The media are provided in unique, light-blocking, temperature-monitored packaging to ensure stability and protect the media from damage by light, contamination, and excessive heat. The media do not require or contain any antimicrobials or phenol red. These components can cause cell stress and influence experimental results by masking the true performance or health of the cell culture. Phenol red acts like an estrogen and may stimulate growth independently of experimental variables. "
New Products: Antibodies, Assays, Small Molecules, Inhibitors, and Proteins
Active Filters
Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.
Entre em contato com a assistência técnica


