NDUFV2 antibody
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935106861
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name
NDUFV2 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab05636
tested applications
ELISA, WB, IHC
Description
The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes the 24 kDa subunit of complex I, and is involved in electron transfer. Mutations in this gene are implicated in Parkinson's disease, bipolar disorder, schizophrenia, and have been found in one case of early onset hypertrophic cardiomyopathy and encephalopathy. A non-transcribed pseudogene of this locus is found on chromosome 19.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kDa (NDUFV2) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 27 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | P19404 |
| Gene ID | 4729 |
| Alias | NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial (NDUFV2),NADH-ubiquinone oxidoreductase 24 kDa subunit,NDUFV2 |
| Background | Antibody anti-NDUFV2 |
| Status | RUO |
| Note | Mol. Weight 27 kDa |
Descripción
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Human NDUFV2 (NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial) ELISA Kit
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NDUFV2 antibody
The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes the 24 kDa subunit of complex I, and is involved in electron transfer. Mutations in this gene are implicated in Parkinson's disease, bipolar disorder, schizophrenia, and have been found in one case of early onset hypertrophic cardiomyopathy and encephalopathy. A non-transcribed pseudogene of this locus is found on chromosome 19.
Ver Producto