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查看说明书Recombinant Glucose-6-phosphate Dehydrogenase (G6PD)
Cat#:TP02170应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | Glucose 6 Phosphate Dehydrogenase Recombinant Rabbit mAb |
| Cat No.: | RMA02612 |
| Clonality: | Monoclonal |
| Species Reactivity: | Human |
| Tested Applications: | WB, IHC, ICC/IF, FC |
| Recommended Dilution: | WB, IHC, ICC/IF, FC |
| 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 Glucose 6 Phosphate Dehydrogenase |
| Calculated Molecular Weight: | 59 kDa |
| Observed Molecular Weight: | 59 kDa |
| GenBank Accession Number: | P11413 |
| Gene ID (NCBI): | 2539 |
| Synonyms: | G6PD1 |
| Background: | This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Category: | Primary Ab |
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