Recombinant fragment, corresponding to a sequence within amino acids 144-494 of Human GLYCTK (NP_660305).
Shipped at 4°C. Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 20% Glycerol, 0.1M Tris, 0.1M Glycine, pH 7.0
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Immunogen affinity purified
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/500 - 1/3000. Predicted molecular weight: 55 kDa.
Defects in GLYCTK are the cause of D-glyceric aciduria (D-GA) [MIM:220120]. D-GA is a rare metabolic disease characterized by chronic metabolic acidosis and a highly variable clinical phenotype. Clinical features range from an encephalopathic presentation with seizures, microcephaly, severe mental retardation and early death, to milder manifestations with only speech delay or even normal development.
Belongs to the glycerate kinase type-2 family.
Cytoplasm and Cytoplasm. Mitochondrion.
Information by UniProt
CG9886 like antibody
Glycerate kinase antibody
Anti-GLYCTK antibody (ab96500)参考文献
has not yet been referenced specifically in any publications.
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