Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase).
The protein is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein.
Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).
Applications:Suitable for use in Western Blot, ELISA
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：200ul
Host：rabbit
Source Antibody：human
Grade：Affinity Purified
Purity：Purified by Protein A affinity chromatography.
Form：Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.
Specificity：Human, mouse
Isotype：IgG
Calc Applications Abbrev：E WB
Calc Crossreactivity：Hu Mo
Immunogen：GLDC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56~85 amino acids from the N-terminal region of human GLDC.
![GLDC, NT (GLDC, GCSP, Glycine dehydrogenase [decarboxylating], mitochondrial, Glycine cleavage system P protein, Glycine decarboxylase) 200ul](https://aimg.as-1.co.jp/c/84/1326/44/85133520.jpg)