Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to
worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting
immunostaining in relation to complex human pathologies.
TCR Screening Services
Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding.
Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".
Rabbit Polyclonal to Human GJB1 / CX32 / Connexin 32
IHC - Paraffin, Western blot (applications tested for the base form of this product only)
Human GJB1 / CX32 / Connexin 32
Human, Rat (tested or 100% immunogen sequence identity)
Also available conjugated with Sepharose.
IHC - Paraffin (1 µg/ml)
Western blot (1 µg/ml)
(applications tested for the base form of this product only)
Specificity and Use
GJB1 / CX32 / Connexin 32 antibody was raised against synthetic peptide corresponding to a sequence at the middle region of human Connexin 32 (215-231aa), identical to the related mouse and rat sequence.
Human, rat., mouse,. No cross reactivity with other proteins.
GJB1 Antibody, Connexin 32 Antibody, CMTX1 Antibody, Connexin-32 Antibody, CX32 Antibody, Gap junction beta-1 protein Antibody, Gap junction protein beta-1 Antibody, CMTX Antibody
GJB1 / CX32 / Connexin 32 is 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.