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NSJ Bioreagents
SKU:RQ8625
BPNT2 Antibody / Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase
BPNT2 Antibody / Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase
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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.
Specifications
| Family | Primary antibody |
|---|---|
| Formulation | 0.5mg/ml if reconstituted with 0.2ml sterile DI water |
| Format | Antigen affinity purified |
| Host Animal | Rabbit |
| Clonality | Polyclonal (rabbit origin) |
| Isotype | Rabbit IgG |
| Species Reactivity | Human, Mouse, Rat |
| Application | WB, IHC-P, IF, FACS, ELISA |
| Application Details | Western blot: 0.5-1ug/ml,Immunohistochemistry (FFPE): 2-5ug/ml,Immunofluorescence: 5ug/ml,Flow cytometry: 1-3ug/million cells,ELISA: 0.1-0.5ug/ml |
| Application Note | Optimal dilution of the BPNT2 antibody should be determined by the researcher. |
| Localization | Cytoplasm (Golgi) |
| Immunogen | An E.coli-derived human recombinant protein (amino acids D62-E354) was used as the immunogen for the BPNT2 antibody. |
| Buffer | Lyophilized from 1X PBS with 2% Trehalose |
| Purity | Antigen affinity purified |
| Storage | After reconstitution, the BPNT2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing. |
| Limitation | This BPNT2 antibody is available for research use only. |
| Uniprot # | Q9NX62 |
| Status | Available |
| PDF Link | https://www.nsjbio.com/tds-pdf/bpnt2-antibody-rq8625 |
| Title | BPNT2 Antibody / Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase |
| Description | 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. |
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