GJC2 Antibody (N-term)(Ascites)
Mouse Monoclonal Antibody (Mab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, E |
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Primary Accession | Q5T442 |
Other Accession | Q80XF7, Q8BQU6, Q29RK8, Q7ZXS7, A4GG66, A4GVD1, P28229, P36383, Q92052, Q6R4A8, P18861, Q2HJ66, NP_065168.2 |
Reactivity | Human |
Predicted | Bovine, Chicken, Hamster, Zebrafish, Mouse, Pig, Rat, Xenopus |
Host | Mouse |
Clonality | Monoclonal |
Isotype | IgM |
Clone/Animal Names | 391CT6.4.3 |
Calculated MW | 47002 Da |
Antigen Region | 53-78 aa |
Gene ID | 57165 |
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Other Names | Gap junction gamma-2 protein, Connexin-466, Cx466, Connexin-47, Cx47, Gap junction alpha-12 protein, GJC2, GJA12 |
Target/Specificity | This GJC2 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 53-78 amino acids from the N-terminal region of human GJC2. |
Dilution | WB~~1:100~8000 |
Format | Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | GJC2 Antibody (N-term)(Ascites) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | GJC2 |
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Synonyms | GJA12 |
Function | One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. May play a role in myelination in central and peripheral nervous systems. |
Cellular Location | Cell membrane; Multi-pass membrane protein. Cell junction, gap junction |
Tissue Location | Expressed in central nervous system, in sciatic nerve and sural nerve. Also detected in skeletal muscles |
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Background
GJC2 is a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.
References
Ferrell, R.E., et al. Am. J. Hum. Genet. 86(6):943-948(2010)
Wang, J., et al. Brain Dev. 32(3):236-243(2010)
Ishikawa, T., et al. Rinsho Shinkeigaku 50(1):7-11(2010)
Ruf, N., et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B (2), 226-232 (2009) :
Orthmann-Murphy, J.L., et al. Brain 132 (PT 2), 426-438 (2009) :
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