NDUFS6 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5115632-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5115632 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
NDUFS6
Classification
Polyclonal
Conjugate
Unconjugated
Gene
NDUFS6
Gene Alias
BC059730; CI-13kA; CI13KDA; CI-13kD-A; complex I 13kDa subunit A; complex I, mitochondrial respiratory chain, 13-kD subunit; complex I-13kD-A; IP13; Ip13dis; NADH dehydrogenase; NADH dehydrogenase (ubiquinone) Fe-S protein 6; NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial; NADH dehydrogenase Fe-S protein 6; NADH ubiquinone oxidoreductase; NADH:ubiquinone oxidoreductase NDUFS6 subunit; NADH:ubiquinone oxidoreductase subunit S6; NADH-ubiquinone oxidoreductase 13 kDa-A subunit; Ndub13; NDUFS6; RATIp13dis; zgc:103774
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
29478, 407785, 4726
Content And Storage
-20°C
Form
Liquid
Applications
Immunocytochemistry, Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide
Gene Accession No.
O75380, P52503, P52504
Gene Symbols
NDUFS6
Immunogen
A synthesized peptide derived from human NDUFS6(Accession O75380), corresponding to amino acid residues S33-R83.
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 NDUFS6
- This gene encodes a subunit of the NADH:ubiquinone oxidoreductase, which is the first enzyme complex in the electron transport chain of mitochondria
- This complex functions in the transfer of electrons from NADH to the respiratory chain
- The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction
- Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.