Human Beta-type platelet-derived growth factor receptor (PDGFRB) ELISA Kit

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AE28215HU
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Product Name Human Beta-type platelet-derived growth factor receptor (PDGFRB) ELISA Kit
Description PDGFRb is a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer, composed of both platelet-derived growth factor receptor alpha and beta polypeptides. This gene is flanked on chromosome 5 by the genes for granulocyte-macrophage colony-stimulating factor and macrophage-colony stimulating factor receptor; all three genes may be implicated in the 5-q syndrome. A translocation between chromosomes 5 and 12, that fuses this gene to that of the translocation, ETV6, leukemia gene, results in chronic myeloproliferative disorder with eosinophilia. This assay has high sensitivity and excellent specificity for detection of Human PDGFRB. No significant cross-reactivity or interference between Human PDGFRB and analogues was observed.
Synonyms CD140B, JTK12, PDGFR, PDGFR1, CD140 antigen-like family member B|PDGF-R-beta|platelet-derived growth factor receptor beta
Method Sandwich ELISA
Detection Range 0.156-10 ng/mL
Sensitivity 0.054 ng/mL
Reactivity Human
Sample Types Serum, Plasma, Other biological fluids.
Background PDGFRb is a cell surface tyrosine kinase receptor for members of the platelet-derived growth factor family. These growth factors are mitogens for cells of mesenchymal origin. The identity of the growth factor bound to a receptor monomer determines whether the functional receptor is a homodimer or a heterodimer, composed of both platelet-derived growth factor receptor alpha and beta polypeptides. This gene is flanked on chromosome 5 by the genes for granulocyte-macrophage colony-stimulating factor and macrophage-colony stimulating factor receptor; all three genes may be implicated in the 5-q syndrome. A translocation between chromosomes 5 and 12, that fuses this gene to that of the translocation, ETV6, leukemia gene, results in chronic myeloproliferative disorder with eosinophilia.
Supplier Abebio

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