GJC2 anticorps
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- Antigène Voir toutes GJC2 Anticorps
- GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp GJC2 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by peptide affinity chromatography method.
- Immunogène
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human GJC2.
- Top Product
- Discover our top product GJC2 Anticorps primaire
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- Indications d'application
- GJC2 antibody can be used for detection of GJC2 by ELISA at 1:312500. GJC2 antibody can be used for detection of GJC2 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Conseil sur la manipulation
- As with any antibody avoid repeat freeze-thaw cycles.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store GJC2 antibody at -20 °C.
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- Antigène
- GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
- Autre désignation
- GJC2 (GJC2 Produits)
- Synonymes
- anticorps GJA12, anticorps cx47, anticorps gja12, anticorps cx46.6, anticorps pmldar, anticorps MGC146420, anticorps B230382L12Rik, anticorps Cx47, anticorps Gja12, anticorps CX46.6, anticorps HLD2, anticorps LMPH1C, anticorps PMLDAR, anticorps SPG44, anticorps gap junction protein gamma 2, anticorps si:dkey-91f15.1, anticorps gap junction protein, gamma 2, anticorps GJC2, anticorps gjc2, anticorps si:dkey-91f15.1, anticorps Gjc2
- Sujet
- 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 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.
- Poids moléculaire
- 47 kDa
- ID gène
- 57165
- NCBI Accession
- NP_065168
- UniProt
- Q5T442
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