PIMA515921
G6PD Monoclonal Antibody (2H7), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA515921-Each-of-1 | In Stock | ₹ 52,287.50 |
PIMA515921 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 52,287.50
GST (18%): ₹ 9,411.75
Total Price: ₹ 61,699.25
Antigen
G6PD
Classification
Monoclonal
Concentration
Conc. Not Determined
Formulation
ascites with 0.03% sodium azide
Gene Accession No.
P11413
Gene Symbols
G6PD
Immunogen
Purified recombinant fragment of human G6PD expressed in E. Coli.
Regulatory Status
RUO
Gene ID (Entrez)
2539
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
ELISA, Flow Cytometry, Immunohistochemistry, Western Blot
Clone
2H7
Conjugate
Unconjugated
Gene
G6PD
Gene Alias
G28A; G6PD; G6PD1; G6pd-1; G6pdx; Glucose-6-phosphate 1-dehydrogenase; glucose-6-phosphate 1-dehydrogenase X; glucose-6-phosphate dehydrogenase; glucose-6-phosphate dehydrogenase X-linked; Gpdx
Host Species
Mouse
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG1
Related Products
Description
- MA5-15921 targets G6PD in indirect ELISA, FACS, IHC, and WB applications and shows reactivity with Human samples
- The MA5-15921 immunogen is purified recombinant fragment of human G6PD expressed in E
- Coli
- MA5-15921 detects G6PD which has a predicted molecular weight of approximately 59kDa
- 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.