NDUFS7 Polyclonal Antibody (CAB24466)
- SKU:
- CAB24466
- Product Type:
- Antibody
- Antibody Type:
- Polyclonal Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- WB
Frequently bought together:
Description
Product Name: | NDUFS7 Polyclonal Antibody |
SKU: | CAB24466 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 80-160 of human NDUFS7 (NP_077718.3). |
Sequence: | WPMT FGLA CCAV EMMH MAAP RYDM DRFG VVFR ASPR QSDV MIVA GTLT NKMA PALR KVYD QMPE PRYV VSMG SCAN GGGY Y |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:1000 - 1:5000 |
Synonyms: | NDUFS7; CI-20; CI-20KD; MY017; PSST; NADH:ubiquinone oxidoreductase core subunit S7 |
Positive Sample: | A549,HeLa,293T |
Conjugate: | Unconjugated |
Cellular Localization: | Mitochondrion. |
Calculated MW: | 22kDa/23kDa |
Observed MW: | 20kDa |
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.
Purification Method: | Affinity purification |
Gene ID: | 374291 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.05% proclin300,50% glycerol,pH7.3. |