NDUFS7 Antibody

Product: Eldecalcitol

NDUFS7 Antibody Summary

Immunogen
Peptide with sequence C-SRGEYVVAKLD corresponding to internal region according to NP_077718.3.
Epitope
SRGEYVVAKLD – internal region
Clonality
Polyclonal
Host
Goat
Gene
NDUFS7
Purity
Immunogen affinity purified
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Applications/Dilutions

Dilutions
  • Western Blot 1 – 3 ug/ml
  • Immunoprecipitation 1:10 – 1:500
  • Peptide ELISA Detection limit 1:16000
Application Notes
WB: Approx. 20 kDa band observed in human heart and human skeletal muscle lysates (calculated MW of 23.6 kDa band according to NP_077718.3).
Publications
Read Publication using NBP1-49846.

Reactivity Notes

Predicted cross-reactivity based on sequence identity: Mouse, Rat, Canine, Bovine.

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
0.5 mg/ml Tris (pH 7.3) and 0.5% BSA
Preservative
0.02% Sodium Azide
Concentration
0.5 mg/ml
Purity
Immunogen affinity purified

Alternate Names for NDUFS7 Antibody

  • CI-20
  • CI-20kD
  • complex I, mitochondrial respiratory chain, 20-KD subunit
  • Complex I-20kD
  • EC 1.6.5.3
  • EC 1.6.99.3
  • EC 1.6.99.5
  • FLJ45860
  • FLJ46880
  • MGC120002
  • MY017
  • NADH dehydrogenase (ubiquinone) Fe-S protein 7 (20kD) (NADH-coenzyme Qreductase)
  • NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Qreductase)
  • NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial
  • NADH:ubiquinone oxidoreductase PSST subunit
  • NADH-coenzyme Q reductase
  • NADH-ubiquinone oxidoreductase 20 kDa subunit
  • PSST subunit
  • PSSTcomplex I 20kDa subunit

Background

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. [provided by RefSeq]

PMID: 8048941