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TMEM231 Antibody (V-17): sc-249021

 |  Datasheet

(Based on data analysis)

  • TMEM231 Antibody (V-17) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping within an internal region of TMEM231 of mouse origin
  • recommended for detection of TMEM231 of mouse, rat and human origin by WB, IF and ELISA; non cross-reactive with other TMEM family members; also reactive with additional species, including equine, canine, bovine and porcine
  • blocking peptide, sc-249021 P
 

See additional TMEM231 Antibodies.

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 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
TMEM231 Antibody (V-17) sc-249021 200 µg/ml $279
TMEM231 (V-17) P sc-249021 P
(peptide)
100 µg/0.5 ml $61
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human TMEM231 79583 16q23.1 NM_001077416, NM_001077418, NM_001077419 Q9H6L2
Mouse Tmem231 234740 8 E1 NM_001033321 Q3U284
N/A
 


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.