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查看说明书Recombinant Human ARG1 Protein
Cat#:TP01213应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | Liver Arginase Rabbit pAb |
| Cat No.: | DPA03541 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human |
| Tested Applications: | WB,IHC,ICC/IF,IP |
| Recommended Dilution: | WB: 1:1000-1:5000 IHC: 1:20 ICC/IF: 1:20 IP: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | A synthetic peptide of human Liver Arginase |
| Calculated Molecular Weight: | 35 kDa |
| Observed Molecular Weight: | 35 kDa |
| GenBank Accession Number: | P05089 |
| Gene ID (NCBI): | 383 |
| Synonyms: | Liver-type arginase; Type I arginase |
| Background: | Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
| Category: | Primary Ab |
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