G6PD polyclonal antibody
Referencia BS6611
embalaje : 100ul
Marca : Bioworld Technology
| Product Name | G6PD polyclonal antibody |
| Catalog No. | BS6611 |
| Swiss-Prot | P11413 |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB, IF/ICC |
| Application_all | WB,1:500 - 1:2000|IF/ICC,1:50 - 1:200 |
| BiowMW | 59KDa |
| Alternative Name | G6PD;G6PD1 |
| Purification&Purity | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE). |
| Conjugate | Unconjugated |
| Modification | Unmodification |
Product Name :
G6PD polyclonal antibody 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. Product :
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2 Storage&Stability :
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles. Specificity :
Polyclonal Antibodies Immunogen :
Recombinant fusion protein of human G6PD(NP_001035810.1). Conjugate :
Unconjugated Modification :
Unmodification
G6PD polyclonal antibody 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. Product :
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2 Storage&Stability :
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles. Specificity :
Polyclonal Antibodies Immunogen :
Recombinant fusion protein of human G6PD(NP_001035810.1). Conjugate :
Unconjugated Modification :
Unmodification


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