GCSH Polyclonal Antibody | G-AB-06785

GCSH Polyclonal Antibody | G-AB-06785 | Gentaur Antibodies

Overview: 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 encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH) . Two transcript variants, one protein-coding and the other probably not protein-coding, have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.

Category Type: Polyclonal Antibody

Research Areas: Cancer, Metabolism, Signal Transduction, Tags & Cell Markers

Synonyms: GCE, GCSH, GCSH, Glycine cleavage system H protein, Glycine cleavage system H protein mitochondrial, Glycine cleavage system protein H (aminomethyl carrier) , Glycine cleavage system protein H, Lipoic acid containing protein, mitochondrial, Mitochondrial glycine cleavage system H protein, NKH

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: BC000790

Clonality: Polyclonal

Immunogen: Fusion protein of human GCSH

Clone #:

Conjugation: Unconjugated

Swissprot: P23434

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1.08 mg/mL

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Purification method: Antigen affinity purification

Application: IHC, ELISA

Dilution: IHC 1:50-1:200, ELISA 1:5000-1:10000

Storage: Store at -20°C. Avoid freeze / thaw cycles.

GCSH Polyclonal Antibody DataSheet