For the best experience on the Abcam website please upgrade to a modern browser such as
Rabbit polyclonal to GLYCTK
Predicted to work with:
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, 1.21% Tris, 0.75% Glycine
Concentration information loading...
Immunogen affinity purified
Abpromise guarantee covers the use of
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.
Involvement in disease
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
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"