GJC2 anticorps (N-Term)
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- Antigène Voir toutes GJC2 Anticorps
- GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
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Épitope
- AA 32-61, N-Term
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Reactivité
- Humain
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Hôte
- Souris
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp GJC2 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- This antibody is prepared by Euglobin precipitation followed by dialysis against PBS.
- Immunogène
- 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
- Top Product
- Discover our top product GJC2 Anticorps primaire
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- Indications d'application
- WB: 1:100~500
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- GJC2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
- Date de péremption
- 6 months
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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.
- Poids moléculaire
- 47002
- ID gène
- 57165
- NCBI Accession
- NP_065168
- UniProt
- Q5T442
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