Mouse Anti-ERBB3 Recombinant Antibody (CBFYE-1127) (CBMAB-E1679-FY)

Basic Information
Application | Note |
IHC-P | 3 µg/ml |
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
May also be activated by CSPG5 (PubMed:15358134).
Involved in the regulation of myeloid cell differentiation (PubMed:27416908).
Extrinsic apoptotic signaling pathway in absence of ligand Source: BHF-UCL
Heart development Source: BHF-UCL
Negative regulation of cell adhesion Source: BHF-UCL
Negative regulation of neuron apoptotic process Source: BHF-UCL
Negative regulation of secretion Source: BHF-UCL
Negative regulation of signal transduction Source: BHF-UCL
Nervous system development Source: GO_Central
Neuron apoptotic process Source: BHF-UCL
Peripheral nervous system development Source: BHF-UCL
Phosphatidylinositol 3-kinase signaling Source: BHF-UCL
Positive regulation of cell population proliferation Source: GO_Central
Positive regulation of kinase activity Source: GO_Central
Positive regulation of phosphatidylinositol 3-kinase signaling Source: BHF-UCL
Positive regulation of protein tyrosine kinase activity Source: BHF-UCL
Regulation of cell population proliferation Source: BHF-UCL
Schwann cell differentiation Source: BHF-UCL
Signal transduction Source: UniProtKB
Transmembrane receptor protein tyrosine kinase signaling pathway Source: BHF-UCL
Wound healing Source: BHF-UCL
Isoform 2: Secreted
A form of lethal congenital contracture syndrome, an autosomal recessive disorder characterized by degeneration of anterior horn neurons, extreme skeletal muscle atrophy, and congenital non-progressive joint contractures (arthrogryposis). The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth. LCCS2 patients manifest craniofacial/ocular findings, lack of hydrops, multiple pterygia, and fractures, as well as a normal duration of pregnancy and a unique feature of a markedly distended urinary bladder (neurogenic bladder defect). The phenotype suggests a spinal cord neuropathic etiology.
Erythroleukemia, familial (FERLK):
An autosomal dominant myeloproliferative disorder characterized by neoplastic proliferation of erythroblastic and myeloblastic elements with atypical erythroblasts and myeloblasts in the peripheral blood. Disease penetrance is incomplete.
Helical: 644-664
Cytoplasmic: 665-1342
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols
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Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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