G6PD Rabbit Polyclonal Antibody (CAB13983)
- SKU:
- CAB13983
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Frequently bought together:
Description
Product Name: | G6PD Rabbit Polyclonal Antibody |
SKU: | CAB13983 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 415-515 of human G6PD (NP_001035810.1). |
Sequence: | PEES ELDL TYGN RYKN VKLP DAYE RLIL DVFC GSQM HFVR SDEL REAW RIFT PLLH QIEL EKPK PIPY IYGS RGPT EADE LMKR VGFQ YEGT YKWV NPHK L |
Tested Applications: | WB IF/ICC ELISA |
Recommended Dilution: | WB,1:500 - 1:1000 IF/ICC,1:50 - 1:200 |
Synonyms: | G6PD1; G6PD |
Positive Sample: | HeLa,C6 |
Conjugate: | Unconjugated |
Cellular Localization: | cytoplasm, cytoplasmic side of plasma membrane, cytosol, extracellular exosome, nucleus |
Calculated MW: | 59kDa |
Observed MW: | 60kDa |
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.
Purification Method: | Affinity purification |
Gene ID: | 2539 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.05% proclin300,50% glycerol,pH7.3. |