Thermo Fisher Scientific NDUFS7 Polyclonal Antibody
NDUFS7 단백질을 인식하는 Thermo Fisher Scientific의 염소 유래 폴리클로날 항체. Western blot 및 IHC(P)에서 검증됨. 인간에 반응하며, 서열 상으로 소, 개, 생쥐, 쥐에도 반응 예측. 미토콘드리아 복합체 I 연구용으로 적합.
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Applications and Tested Dilution
| Application | Tested Dilution | Publications |
|---|---|---|
| Western Blot (WB) | 1–3 µg/mL | View 3 publications |
| Immunohistochemistry (Paraffin) (IHC (P)) | 5 µg/mL | - |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Published Species | Mouse, Rat |
| Host / Isotype | Goat / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide sequence (SRGEYVVAKLD) corresponding to the internal amino acids of NDUFS7 (aa 58–69) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Ammonium sulfate precipitation |
| Storage Buffer | TBS, pH 7.3, with 0.5% BSA |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Wet ice |
| RRID | AB_10979884 |
Product Specific Information
- Predicted to react with bovine, canine, mouse, and rat based on sequence homology.
- Tested in Peptide ELISA: antibody detection limit dilution 1:16,000.
Target Information
This gene encodes a protein that is a subunit of one of the complexes forming the mitochondrial respiratory chain. It is part of complex I (NADH:ubiquinone oxidoreductase), which transfers electrons from NADH to the respiratory chain, with ubiquinone as the immediate electron acceptor.
Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder characterized by 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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