BPNT2 Antilichaam / Golgi-ingezeten adenosine 3',5'-bisfosfaat 3'-fosfatase

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP) . Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Western blot: 0.5-1 µg/mL, Immunohistochemistry (FFPE) : 2-5 µg/mL, Immunofluorescence: 5 µg/mL, Flow cytometry: 1-3ug/million cells, ELISA: 0.1-0.5 µg/mL

Q9NX62

Human, Mouse, Rat

An E.coli-derived human recombinant protein (amino acids D62-E354) was used as the immunogen for the BPNT2 antibody.

WB, IHC-P, IF, FACS, ELISA

Antigen affinity purified

Antigen affinity purified

Lyophilized from 1X PBS with 2% Trehalose

This BPNT2 antibody is available for research use only.

After reconstitution, the BPNT2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

0.5 mg/mL if reconstituted with 0.2ml sterile DI water

Optimal dilution of the BPNT2 antibody should be determined by the researcher.

Cytoplasm (Golgi)

IHC staining of FFPE human lung cancer tissue with BPNT2 antibody. HIER: boil tissue sections in pH8 EDTA for 20 min and allow to cool before testing.