PDGF Receptor alpha (PDGFRA) Mouse Monoclonal Antibody [Clone ID: 16A1]
CAT#: AM12068BT-N
PDGF Receptor alpha (PDGFRA) mouse monoclonal antibody, clone 16A1, Biotin
Conjugation: Unconjugated APC PE
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CNY 3,810.00
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Specifications
Product Data | |
Clone Name | 16A1 |
Applications | FC |
Recommend Dilution | Indirect immunofluorescence analysis by Flow cytometry: 3 μg/ml as starting dilution. |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | CD140a-transfected NIH 3T3 cells |
Specificity | The antibody recognizes CD140a / PDGF-RA, the 170 kDa alpha chain of platelet-derived growth factor receptor, which is widely expressed on a variety of mesenchymal-derived cells and plays pro-proliferative or anti-proliferative roles in various tumours. |
Formulation | Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.4 Label: Biotin State: Liquid purified Ig fraction Label: Conjugated with -LC-NHS under optimum conditions. The reagent is free of unconjugated biotin |
Concentration | lot specific |
Conjugation | Biotin |
Storage Condition | Store the antibody undiluted at 2 - 8 °C. DO NOT FREEZE! |
Gene Name | platelet derived growth factor receptor alpha |
Database Link | |
Background | CD140a / PDGF-RA (platelet-derived growth factor receptor alpha) is a cell surface receptor for members of platelet-derived growth factor family, whose intracellular part contains a tyrosine kinase domain. CD140a forms homodimers, or heterodimerizes with CD140b / PDGF-RB. Whereas CD140b induces in different cell types their proliferation and migration, the role of CD140a is more controversial, with pro-proliferative or anti-proliferative effects. CD140a has early developmental functions, mediates mesodermal cell migration, and later acts in signaling associated in epithelial-mesenchymal interactions. |
Synonyms | PDGF-R-alpha, PDGF Receptor alpha |
Reference Data | |
Protein Families | Druggable Genome, ES Cell Differentiation/IPS, Protein Kinase, Transmembrane |
Protein Pathways | Calcium signaling pathway, Colorectal cancer, Cytokine-cytokine receptor interaction, Endocytosis, Focal adhesion, Gap junction, Glioma, MAPK signaling pathway, Melanoma, Pathways in cancer, Prostate cancer, Regulation of actin cytoskeleton |
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