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MS4A8B Antibody (V-15): sc-240716

 |  Datasheet

(Based on data analysis)
  • MS4A8B Antibody (V-15) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping within a cytoplasmic domain of MS4A8B of mouse origin
  • recommended for detection of MS4A8B of mouse and rat origin by WB, IF and ELISA; non cross-reactive with other MS4A family members
  • blocking peptide, sc-240716 P
 

See additional MS4 Antibodies including MS4, MS4A13, MS4A14, MS4A3, MS4A4, MS4A4A, MS4A6A, MS4A5, MS4A7, MS4A8B, MS4A10, MS4A12 and MS4A15.

Ordering InformationGene Info
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 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
MS4A8B Antibody (V-15) sc-240716 200 µg/ml $279
MS4A8B (V-15) P sc-240716 P
(peptide)
 100 µg/0.5 ml $61
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Mouse Ms4a8a 64381 19 A NM_022430 Q99N10
 N/A
 

MS4A (membrane-spanning 4-domain family, subfamily A) is a large family of proteins that includes at least 26 members in mouse and humans. Flanked by amino- and carboxyl- cytoplasmic regions, MS4A family members contain four highly conserved transmembrane domains. MS4A8B (membrane-spanning 4-domains, subfamily A, member 8B), also known as 4SPAN4 (four-span transmembrane protein 4), is a 250 amino acid multi-pass membrane protein that is expressed in hematopoietic cells and tissue. The gene encoding MS4A8B maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.