NT5C3 rabbit pAb
ENT-A6343
Description
| REF | ENT-A6343 |
|---|---|
| Category | Antibody Polyclonal |
| Description | NT5C3 rabbit pAb |
| Source | Rabbit |
| Applications | WB;IHC;IF;ELISA |
| Reactivity | Human;Mouse |
| Reactivity | Human;Mouse |
| Dilution | 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 Stability | -20°C/1 year |
| Clonality | Polyclonal |
| Isotype | IgG |
| Concentration | 1 mg/ml |
| Observed Band KD | 38kD |
| Human Gene ID | 51251 |
| Human Swiss Prot Nº | Q9H0P0 |
| Subcellular Location | Cytoplasm .; [Isoform 2]: Endoplasmic reticulum. |
Other Name: 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
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],