Thermo Fisher Scientific NDUFS7 Monoclonal Antibody (3A3)
NDUFS7 단백질을 인식하는 Thermo Fisher의 Mouse Monoclonal Antibody(3A3). Human 시료에 반응하며 ELISA에 적합. Affinity chromatography로 정제된 액상 항체로, 보존제가 없으며 -20°C에서 보관. 연구용으로만 사용 가능.
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Applications
- ELISA (ELISA)
Tested Dilution: 10 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG2b, kappa |
| Class | Monoclonal |
| Type | Antibody |
| Clone | 3A3 |
| Immunogen | NDUFS7 (NP_077718, 114 a.a. ~ 213 a.a.) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | See Label |
| Purification | Affinity chromatography |
| Storage buffer | PBS, pH 7.4 |
| Contains | No preservative |
| Storage conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
Sequence of this protein is as follows:
PRQSDVMIVA GTLTNKMAPA LRKVYDQMPE PRYVVSMGSC ANGGGYYHYS YSVVRGCDRI VPVDIYIPGC PPTAEALLYG ILQLQRKIKR ERRLQIWYRR
Target Information
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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