GCSH Polyclonal Antibody | G-AB-08402

GCSH Polyclonal Antibody | G-AB-08402 | 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: GCSH, GCE, NKH

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID: 2653

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human GCSH (NP_004474.2) .

Clone #:

Conjugation: Unconjugated

Swissprot: P23434

Santa Cruz:

Calculated MW: 18 kDa

Observed MW: 19 kDa

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: WB, IF

Dilution: WB 1:500-1:2000 IF 1:50-1:200

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

GCSH Polyclonal Antibody DataSheet