GJB1 antibody (Middle Region)
Quick Overview for GJB1 antibody (Middle Region) (ABIN7992683)
Target
See all GJB1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
Grade
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Binding Specificity
- Middle Region
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Purpose
- Anti-Connexin 32/GJB1 Antibody
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Specificity
- No cross reactivity with other proteins.
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Cross-Reactivity (Details)
- No cross-reactivity with other proteins.
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Predicted Reactivity
- identical to the related mouse,rat sequences.
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Characteristics
- Anti-Connexin 32/GJB1 Antibody. Tested in WB applications. This antibody reacts with Mouse, Rat.
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Purification
- Immunogen affinity purified.
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Immunogen
- A synthetic peptide corresponding to a sequence in the middle region of human Connexin 32/GJB1, identical to the related mouse and rat sequences.
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Isotype
- IgG
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Application Notes
- Western blot, 0.1-0.5 μg/mL
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg NaN3.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- 4 °C,-20 °C
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Storage Comment
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles. -
Expiry Date
- 12 months
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- GJB1 (Gap Junction Protein, beta 1, 32kDa (GJB1))
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Alternative Name
- GJB1
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Background
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Background: Gap junction beta-1 protein (GJB1), also known as connexin 32 (Cx32) is a transmembrane protein that in humans is encoded by the GJB1 gene. This gene encodes a member of the gap junction protein family. The gap junction proteins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
Gene Full Name: gap junction protein beta 1
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Molecular Weight
- 32 kDa
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Gene ID
- 2705
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UniProt
- P08034
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Pathways
- Cell-Cell Junction Organization
Target
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