Canine NRG1-alpha Protein (EGF Domain, Fc Tag)
NRG1
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Catalog Number | P70084-D04H |
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Organism Species | Canine |
Host | Human Cells |
Synonyms | NRG1 |
Molecular Weight | The recombinant canine NRG1 is a disulfide-linked homodimer. The reduced monomer comprises 301 amino acids and has a predicted molecular mass of 34 kDa. The apparent molecular mass of the protein is approximately 37 and 34 kDa in SDS-PAGE under reducing conditions. |
predicted N | Asp |
SDS-PAGE | |
Purity | (92.0+7.0) % as determined by SDS-PAGE |
Protein Construction | A DNA sequence encoding the canine NRG1 isoform alpha (XP_858147.1) EGF-like domain (Ser176-Lys240) was expressed with the Fc region of mouse IgG1 at the N-terminus. |
Bio-activity | Measured in a serum-free cell proliferation assay using MCF‑7 human breast cancer cells. The ED50 for this effect is typically 0.1-1 µg/mL. |
Research Area | Immunology |Signal Transduction |Nuclear signaling |Nuclear Hormone Receptor |Co-activator & Co-repressor |
Formulation | Lyophilized from sterile PBS, pH 7.4. 1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA. |
Background | Neuregulin 1 or NRG1 is one of four proteins in the neuregulin family that act on the EGFR family of receptors. This growth factor was originally identified as a 44-kD glycoprotein that interacts with the NEU / ERBB2 receptor tyrosine kinase to increase its phosphorylation on tyrosine residues. NRG1 is a trophic factor that has been implicated in neural development, neurotransmission, and synaptic plasticity. NRG1 has multiple isoforms that are generated by usage of different promoters and alternative splicing of a single gene. Neuregulin 1 (NRG1) is essential for the development and function of multiple organ systems, and its dysregulation has been linked to diseases such as cancer and schizophrenia. NRG1 is a schizophrenia candidate gene and plays an important role in brain development and neural function. Schizophrenia is a complex disorder, with etiology likely due to epistasis. |
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