ETFA Antibody

ProSci
Product Code: PSI-26-842
Product Group: Primary Antibodies
Supplier: ProSci
CodeSizePrice
PSI-26-842-100ul100ul£662.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
  • Human
  • Mouse
  • Rat
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Western Blot (WB)
Storage:
For short periods of storage (days) store at 4˚C. For longer periods of storage, store ETFA antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.

Images

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Antibody used in WB on Human Heart at 0.2-1 ug/ml.
2 / 4
3 / 4
Antibody used in WB on Human Hela at 1 ug/ml.
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Antibody used in WB on Hum. Fetal Liver at 1 ug/ml.

Antibody used in WB on Human Heart at 0.2-1 ug/ml.
Antibody used in WB on Human Hela at 1 ug/ml.
Antibody used in WB on Hum. Fetal Liver at 1 ug/ml.

Further Information

Additional Names:
ETFA, EMA, GA2, MADD
Application Note:
ETFA antibody can be used for detection of ETFA by ELISA at 1:62500. ETFA antibody can be used for detection of ETFA by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Background:
ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids.ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene.
Background References:
  • Chiong, M.A., Mol. Genet. Metab. 92 (1-2), 109-114 (2007).
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Conjugate:
Unconjugated
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ETFA.
NCBI Gene ID #:
2108
NCBI Official Name:
electron-transfer-flavoprotein, alpha polypeptide
NCBI Official Symbol:
ETFA
NCBI Organism:
Homo sapiens
Physical State:
Liquid
PREDICTED MOLECULAR WEIGHT:
35 kDa
Protein Accession #:
NP_000117
Protein GI Number:
4503607
Purification:
Antibody is purified by peptide affinity chromatography method.
Swissprot #:
P13804
User NOte:
Optimal dilutions for each application to be determined by the researcher.