GJB1 polyclonal antibody
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More Files
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Western Blot
Western blot analysis of tissue and whole cell extracts with GJB1 polyclonal antibody (Cat # PAB19101).
Lane 1 : rat heart. Lane 2 : rat skeletal muscle. Lane 3 : rat barin.
Lane 4 : MM231. Lane 5 : HeLa. Lane 6 : SMMC. Lane 7 : HT1060.
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of GJB1.
Immunogen
A synthetic peptide corresponding to internal region of human GJB1.
Host
Rabbit
Reactivity
Human, Rat
Form
Lyophilized
Purification
Immunoaffinity purification
Isotype
IgG
Recommend Usage
Western Blot (1 ug/mL)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
Lyophilized from 0.9 mg NaCl, 0.2 mg Na2HPO4 (5 mg BSA, 0.05 mg sodium azide, 0.05 mg Thimerosal)
Storage Instruction
Store at -20°C on dry atmosphere.
After reconstitution with 200 uL of deionized water and concentration will be 500 ug/mL, store at -20°C or lower.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide and thimerosal: POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot
Western blot analysis of tissue and whole cell extracts with GJB1 polyclonal antibody (Cat # PAB19101).
Lane 1 : rat heart. Lane 2 : rat skeletal muscle. Lane 3 : rat barin.
Lane 4 : MM231. Lane 5 : HeLa. Lane 6 : SMMC. Lane 7 : HT1060.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
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Gene Info — GJB1
Entrez GeneID
2705Gene Name
GJB1
Gene Alias
CMTX, CMTX1, CX32
Gene Description
gap junction protein, beta 1, 32kDa
Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
OTTHUMP00000023502|OTTHUMP00000023503|OTTHUMP00000023504|connexin 32
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Interactome
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Disease
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