CD167a (DDR1), Human Antibody from MILTENYI BIOTEC B.V. & Co. KG

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Antigenic SpecificityCD167a (DDR1), Human
Clone51D6
Host SpeciesMouse
Reactive Specieshuman
IsotypeIgG3κ
Formatbiotin conjugate
Size30 tests in 300 µL
Concentration1:11
ApplicationsFlow cytometry
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DescriptionCD167a (DDR1) Antibody, anti-human, Biotin. Clone 51D6 recognizes the human CD167a antigen, a single-pass type I membrane protein, which is also known as discoidin domain receptor (DDR1), mammary carcinoma kinase 10 (MCK-10), or tyrosine kinase receptor E (trkE). CD167a is a tyrosine kinase that functions as cell surface receptor for fibrillar collagen and regulates cell attachment to the extracellular matrix, remodeling of the extracellular matrix, cell migration, differentiation, survival, and cell proliferation. It promotes smooth muscle cell migration, and thereby contributes to arterial wound healing. CD167a also plays a role in tumor cell invasion. Three isoforms of CD167a have been reported. CD167a is expressed on epithelial cells, keratinocytes, leukocytes, monocytes, and has been reported to be overexpressed in some breast carcinomas. |
Immunogenn/a
Other NamesHGK2, MCK-10, RTK-6, TRK E, DDR, CAK
Gene, Accession #Gene ID: 780
Catalog #130-110-122
Price$88
Order / More InfoCD167a (DDR1), Human Antibody from MILTENYI BIOTEC B.V. & Co. KG
Product Specific ReferencesDi Marco, E. et al. (1993) Molecular cloning of trkE, a novel trk-related putative tyrosine kinase receptor isolated from normal human keratinocytes and widely expressed by normal human tissues. J. Biol. Chem. 268 (32): 2490-2495. | Canning, P. et al. (2014) Structural mechanisms determining inhibition of the collagen receptor DDR1 by selective and multi-targeted type II kinase inhibitors. J. Mol. Biol. 426 (13): 2457-2470. | Hohenester, E. (2014) Signalling complexes at the cell-matrix interface. Curr. Opin. Struct. Biol. 29C: 10-16.
MILTENYI BIOTEC B.V. & Co. KG
MILTENYI BIOTEC B.V. & Co. KG
MILTENYI BIOTEC B.V. & Co. KG
Friedrich-Ebert-Straße 68
51429 Bergisch Gladbach GERMANY
P: +49 2204 8306-0
F: +49 2204 85197

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