NDUFS7 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5106367-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5106367 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
NDUFS7
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Ndufs7
Gene Alias
1010001M04Rik; CI-20; CI-20KD; complex I 20kDa subunit; complex I, mitochondrial respiratory chain, 20-KD subunit; complex I-20kD; FLJ45860; FLJ46880; MGC120002; MY017; NADH dehydrogenase (ubiquinone) Fe-S protein 7; NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial; NADH:ubiquinone oxidoreductase core subunit S7; NADH:ubiquinone oxidoreductase PSST subunit; NADH-coenzyme Q reductase; NADH-ubiquinone oxidoreductase 20 kDa subunit; NADH-ubiquinone oxidoreductase Fe-S protein 7; NDUFS7; PSST; PSST subunit
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
362837, 374291, 75406
Content And Storage
-20°C
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
O75251, Q9DC70
Gene Symbols
Ndufs7
Immunogen
A synthesized peptide derived from human NDUFS7(Accession O75251), corresponding to amino acid residues G38-C88.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antibody detects endogenous levels of total NDUFS7
- This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain
- This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase
- This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme
- Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.