Hu, Mu, Rt, Bv, Ca, Ch, ChHaApplications:
WB, ICC/IF, IHC, IHC-Fr, IHC-PHost:
Hu, Mu, Rt, Po, BvApplications:
WB, Flow, ICC/IF, PEP-ELISAHost:
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
Applications: WB, ELISA, PA, AP
58K protein antibodies are excellent for use as markers for the Golgi complex. The 58K protein has been identified as being FTCD, a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Defects in FTCD are the cause of glutamate formiminotransferase deficiency; also known as formiminoglutamicaciduria (FIGLU-uria). It is an autosomal recessive disorder. Features of a severe phenotype, include elevated levels of formiminoglutamate (FIGLU) in the urine in response to histidine administration, megaloblastic anemia, and mental retardation. Features of a mild phenotype include high urinary excretion of FIGLU in the absence of histidine administration, mild developmental delay, and no hematological abnormalities.
PTMs for 58K Golgi Protein
Learn more about PTMs related to 58K Golgi Protein.MethylationCleavage
Bioinformatics Tool for 58K Golgi Protein
Discover related pathways, diseases and genes to 58K Golgi Protein. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.