ProductsBack/Citrate synthase antibody [GT1761]

Citrate synthase antibody [GT1761]

Name: Citrate synthase antibody [GT1761]
SKU: GTX628143_G10
Availability: BackOrder

GTX628143

ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin

Product group Antibodies

TargetCS

Overview

Supplier
GeneTex
Product Name
Citrate synthase antibody [GT1761]
Delivery Days Customer
9
Application Supplier Note
WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
Applications
ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Certification
Research Use Only
Clonality
Monoclonal
Clone ID
GT1761
Concentration
1 mg/ml
Conjugate
Unconjugated
Gene ID1431
Target name
CS
Target description
citrate synthase
Target synonyms
citrate synthase, mitochondrial, citrate (Si)-synthase
Host
Mouse
Isotype
IgG2a
Protein IDO75390
Protein Name
Citrate synthase, mitochondrial
Scientific Description
The 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]
Storage Instruction
-20°C or -80°C,2°C to 8°C
UNSPSC
12352203

Ranea-Robles P, Portman K, Bender A, et al. Peroxisomal L-bifunctional protein (EHHADH) deficiency causes male-specific kidney hypertrophy and proximal tubular injury in mice. Kidney360. 2021,2(9):1441-1454. doi: 10.34067/KID.0003772021
Read this paper
Ranea-Robles P, Violante S, Argmann C, et al. Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis. Cell Mol Life Sci. 2021,78(14):5631-5646. doi: 10.1007/s00018-021-03869-9
Read this paper
Zhang X, Nemeria NS, Leandro J, et al. Structure-function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism. J Biol Chem. 2020,295(23):8078-8095. doi: 10.1074/jbc.RA120.012761
Read this paper
Leandro J, Dodatko T, Aten J, et al. DHTKD1 and OGDH display substrate overlap in cultured cells and form a hybrid 2-oxo acid dehydrogenase complex in vivo. Hum Mol Genet. 2020,29(7):1168-1179. doi: 10.1093/hmg/ddaa037
Read this paper
Baati N, Feillet-Coudray C, Fouret G, et al. New evidence of exercise training benefits in myostatin-deficient mice: Effect on lipidomic abnormalities. Biochem Biophys Res Commun. 2019,516(1):89-95. doi: 10.1016/j.bbrc.2019.06.014
Read this paper