OXCT1 Antibody Cat

OXCT1 Antibody Cat

OXCT1 Antibody Cat. No.: 30-414 OXCT1 Antibody Antibody used in WB on Hum. Adult Placenta at 1 ug/ml. Specifications HOST SPECIES: Rabbit SPECIES REACTIVITY: Human, Mouse, Rat Antibody produced in rabbits immunized with a synthetic peptide corresponding a region IMMUNOGEN: of human OXCT1. TESTED APPLICATIONS: ELISA, WB OXCT1 antibody can be used for detection of OXCT1 by ELISA at 1:62500. OXCT1 antibody APPLICATIONS: can be used for detection of OXCT1 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000. POSITIVE CONTROL: 1) Cat. No. 1201 - HeLa Cell Lysate PREDICTED MOLECULAR 52 kDa WEIGHT: October 2, 2021 1 https://www.prosci-inc.com/oxct1-antibody-30-414.html Properties PURIFICATION: Antibody is purified by peptide affinity chromatography method. CLONALITY: Polyclonal CONJUGATE: Unconjugated PHYSICAL STATE: Liquid Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% BUFFER: sucrose. CONCENTRATION: batch dependent For short periods of storage (days) store at 4˚C. For longer periods of storage, store STORAGE CONDITIONS: OXCT1 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles. Additional Info OFFICIAL SYMBOL: OXCT1 ALTERNATE NAMES: OXCT1, OXCT, SCOT ACCESSION NO.: NP_000427 PROTEIN GI NO.: 4557817 GENE ID: 5019 USER NOTE: Optimal dilutions for each application to be determined by the researcher. Background and References OXCT1 is a member of the 3-oxoacid CoA-transferase gene family. It is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate.This gene encodes a member of the 3-oxoacid CoA-transferase gene family. BACKGROUND: The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency. REFERENCES: 1) Fukao, T., (2007) Mol. Genet. Metab. 92 (3), 216-221. ANTIBODIES FOR RESEARCH USE ONLY. For additional information, visit ProSci's Terms & Conditions Page. October 2, 2021 2 https://www.prosci-inc.com/oxct1-antibody-30-414.html.

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