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GJC2 antibody (N-Term)
GJC2
Reactivity: Human
WB
Host: Mouse
Monoclonal
391CT6-4-3
unconjugated
Product Details anti-GJC2 Antibody
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Target
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GJC2
(Gap Junction Protein, gamma 2, 47kDa (GJC2))
Binding Specificity
All epitopes for GJC2 antibodies
AA 32-61, N-Term
Reactivity
All reactivities for GJC2 antibodies
Human
Host
All hosts for GJC2 antibodies
Mouse
Clonality
All clonalities for GJC2 antibodies
Monoclonal
Conjugate
All conjugates for GJC2 antibodies
This GJC2 antibody is un-conjugated
Application
All applications for GJC2 antibodies
Western Blotting (WB)
Purification
This antibody is prepared by Euglobin precipitation followed by dialysis against PBS.
Immunogen
This GJC2 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 32-61 amino acids from the N-terminal region of human GJC2.
Clone
391CT6-4-3
Isotype
IgM
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Alternatives
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Application Details
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Application Notes
WB: 1:100~500
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
GJC2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
Expiry Date
6 months
Target Details for GJC2
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Target
GJC2
(Gap Junction Protein, gamma 2, 47kDa (GJC2))
Alternative Name
GJC2 (GJC2 Products )
Synonyms
GJA12 antibody, cx47 antibody, gja12 antibody, cx46.6 antibody, pmldar antibody, MGC146420 antibody, B230382L12Rik antibody, Cx47 antibody, Gja12 antibody, CX46.6 antibody, HLD2 antibody, LMPH1C antibody, PMLDAR antibody, SPG44 antibody, gap junction protein gamma 2 antibody, si:dkey-91f15.1 antibody, gap junction protein, gamma 2 antibody, GJC2 antibody, gjc2 antibody, si:dkey-91f15.1 antibody, Gjc2 antibody
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.
Molecular Weight
47002
Gene ID
57165
NCBI Accession
NP_065168
UniProt
Q5T442
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