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TMEM231 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of TMEM231 antibodies. Select TMEM231 antibodies from several monoclonal and/or polyclonal TMEM231 antibodies listed below. View detailed TMEM231 antibody specifications by linking to the specific product blocks. Select appropriate TMEM231 antibodies for your research by isotype, epitope, applications and species reactivity. TMEM231 gene silencer products in siRNA, shRNA Plasmid and shRNA Lentiviral Particle formats are also available.

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a unique system for rapid identification of TMEM231 Antibodies. Hover over product names in the table to see representative data for each product.

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PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
TMEM231 (S-16)sc-249017goat IgGInternal (h)WB, IF, ELISAm, r, h, e, c, b, p
TMEM231 (T-17)sc-249018goat IgGInternal (h)WB, IF, ELISAhuman
TMEM231 (V-17)sc-249021goat IgGInternal (m)WB, IF, ELISAm, r, h, e, c, b, p

TMEM231 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
TMEM231 siRNA (m): sc-140248TMEM231 shRNA Plasmid (m):
sc-140248-SH
TMEM231 shRNA (m)
Lentiviral Particles: sc-140248-V

TMEM231 (transmembrane protein 231), also known as ALYE870 or PRO1886, is a 316 amino acid multi-pass membrane protein that belongs to the TMEM231 family and is encoded by a gene that maps to human chromosome 16q23.1. Chromosome 16 encodes over 900 genes and comprises nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, through the CREBBP gene, which encodes a critical CREB binding protein. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.