ELK Bio
NT5C3 rabbit pAb - ES6506
NT5C3 rabbit pAb - ES6506
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NT5C3 rabbit pAb
Sizes: 50μL, 100μL
Catalogue Numbers: ES6506-50, ES6506-100
Citations, Manuals and MSDS Available upon request.
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],
Alternate 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
Source: Rabbit
Applications: WB; IHC; IF; ELISA
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.
Reactivity: Human; Mouse
Immunogen: The antiserum was produced against synthesized peptide derived from human NT5C3. AA range:11-60
Storage and 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.
Research Use Only
