SH3PXD2B Antibody, Rabbit PAb

Catalog number: HPA036471
Brand: Atlas Antibodies
Packing: 100 ul
Price: € 352.00
Expected delivery time: 7 days
Quantity:

Product specifications for - SH3PXD2B Antibody, Rabbit PAb

Overview: 
Product group: Antibodies
Category: Primary Antibodies
Application: ImmunoHistoChemistry, Western Blot
Host: Rabbit
Target: SH3PXD2B
Target description: SH3 and PX domains 2B
Clonality: Polyclonal
Isotype: IgG
Properties: 
Purity: Purification method: Affinity purified using the PrEST antigen as affinity ligand
Datasheet: Datasheet
  Research Use Only
UNSPSC: 12352203
Form supplied: The antibodies are delivered in 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage instructions: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
Scientific information: 
Scientific info: Specification: This antibody has been used for staining of 48 normal human tissue samples as well as human cancer samples covering the 20 most common cancer types and up to 12 patients for each cancer type.
Gene ID: 285590
Swiss prot ID: A1X283
Related products: 
Related products: Corresponding Atlas Antigen: APrEST80096
Additional information: 
Synonyms: HPA036471; SH3PXD2B; TSK4; TKS4; KIAA1295; HOFI; FTHS; FAD49; tyrosine kinase substrate with four SH3 domains; factor for adipocyte differentiation 49; adaptor protein HOFI; adapter protein HOFI; SH3 and PX domain-containing protein 2B; SH3 and PX domains 2B
Wilson GR, Sunley J, Smith KR, Pope K, Bromhead CJ, Fitzpatrick E, Di Rocco M, van Steensel M, Coman DJ, Leventer RJ, Delatycki MB, Amor DJ, Bahlo M, Lockhart PJ. "Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome". Eur J Hum Genet 2014 Jun; 22(6):741-747. Epub 2013 Oct 9. DOI: 10.1038/ejhg.2013.229. Read more
Marsh AP, Lukic V, Pope K, Bromhead C, Tankard R, Ryan MM, Yiu EM, Sim JC, Delatycki MB, Amor DJ, McGillivray G, Sherr EH, Bahlo M, Leventer RJ, Lockhart PJ. "Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss". Neurol Genet 1/01/01; 1(2):e16. Epub 2015 Jul 16. DOI: 10.1212/NXG.0000000000000014. Read more