| Product name: |
NT5C3 rabbit pAb |
| Reactivity: |
Human;Mouse |
| Alternative Names: |
NT5C3; P5N1; UMPH1; HSPC233; Cytosolic 5′-nucleotidase 3; Cytosolic 5′-nucleotidase III; cN-III; Pyrimidine 5′-nucleotidase 1; P5’N-1; P5N-1; PN-I; Uridine 5′-monophosphate hydrolase 1; p36 |
| Source: |
Rabbit |
| Dilutions: |
Western Blot: 1/500 – 1/2000. Immunohistochemistry: 1/100 – 1/300. Immunofluorescence: 1/200 – 1/1000. ELISA: 1/40000. Not yet tested in other applications. |
| Immunogen: |
The antiserum was produced against synthesized peptide derived from human NT5C3. AA range:11-60 |
| Storage: |
-20C/1 year |
| Clonality: |
Polyclonal |
| Isotype: |
IgG |
| Concentration: |
1 mg/ml |
| Observed Band: |
38kD |
| GeneID: |
51251 |
| Human Swiss-Prot No: |
Q9H0P0 |
| Cellular localization: |
Cytoplasm .; [Isoform 2]: Endoplasmic reticulum. |
| Background: |
5′-nucleotidase, cytosolic IIIA(NT5C3A) Homo sapiens This gene encodes a member of the 5′-nucleotidase family of enzymes that catalyze the dephosphorylation of nucleoside 5′-monophosphates. The encoded protein is the type 1 isozyme of pyrimidine 5′ nucleotidase and catalyzes the dephosphorylation of pyrimidine 5′ monophosphates. Mutations in this gene are a cause of hemolytic anemia due to uridine 5-prime monophosphate hydrolase deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and pseudogenes of this gene are located on the long arm of chromosomes 3 and 4. [provided by RefSeq, Mar 2012], |
