Gap Junction Protein Gamma 2 (GJC2) Antibody

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Description
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. This antibody is supplied as crude ascites.
Documents del producto
Product specifications
Category | Primary Antibodies |
Immunogen Target | Gap Junction Protein Gamma 2 (GJC2) |
Host | Mouse |
Reactivity | Human |
Recommended Dilution | WB: 1/100 - 1/8000. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Monoclonal |
Conjugation | Unconjugated |
Isotype | IgM |
Purification | Unpurified crude ascites. |
Size 1 | 100 µl |
Form | Liquid |
Tested Applications | ELISA, WB |
Buffer | Ascites containing 0.09% sodium azide. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | Q5T442 |
Background | Antibody anti-GJC2 |
Status | RUO |
Descripción
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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.
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Gap Junction Protein Gamma 2 (GJC2) Antibody
GJC2 Antibody is a Rabbit Polyclonal antibody against GJC2. This gene encodes 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.
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Gap Junction Protein Gamma 2 (GJC2) Antibody
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. This antibody is supplied as crude ascites.
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