Citrate synthase antibody [N2C3]
GTX110624
ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityAmphibian, Chicken, Human, Monkey, Mouse, Rat, Zebra Fish
TargetCS
Overview
- SupplierGeneTex
- Product NameCitrate synthase antibody [N2C3]
- Delivery Days Customer9
- Application Supplier NoteWB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration0.65 mg/ml
- ConjugateUnconjugated
- FormulationLiquid
- Gene ID1431
- Target nameCS
- Target descriptioncitrate synthase
- Target synonymscitrate (Si)-synthase; citrate synthase, mitochondrial
- HostRabbit
- IsotypeIgG
- Protein IDO75390
- Protein NameCitrate synthase, mitochondrial
- Scientific DescriptionThe protein encoded by this gene is a Krebs tricarboxylic acid cycle enzyme that catalyzes the synthesis of citrate from oxaloacetate and acetyl coenzyme A. The enzyme is found in nearly all cells capable of oxidative metablism. This protein is nuclear encoded and transported into the mitochondrial matrix, where the mature form is found. [provided by RefSeq]
- ReactivityAmphibian, Chicken, Human, Monkey, Mouse, Rat, Zebra Fish
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203
References
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- Mild inborn errors of metabolism in commonly used inbred mouse strains. Leandro J et al., 2019 Apr, Mol Genet MetabRead more
- Effects of long-term exposures to low iron and branched-chain amino acid containing diets on aging skeletal muscle of Fisher 344 x Brown Norway rats. Kim Y et al., 2018 Feb, Appl Physiol Nutr MetabRead more
- Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome. Lake NJ et al., 2017 Aug 3, Am J Hum GenetRead more
- Myostatin deficiency is associated with lipidomic abnormalities in skeletal muscles. Baati N et al., 2017 Oct, Biochim Biophys Acta Mol Cell Biol LipidsRead more
- Mitochondrial retrograde signaling connects respiratory capacity to thermogenic gene expression. Nam M et al., 2017 May 17, Sci RepRead more