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GCSH Polyclonal Antibody

CAT: 0866-RD81570A-01Size: 60 μLDry Ice: NoHazardous: No
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CAT#:0866-RD81570A-01Size:60 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
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.
Description
This is a GCSH Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
Synonyms
GCSH, GCE, NKH
Gene ID
2653
Swiss Prot
P23434
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein of human GCSH (NP_004474.2) .
Conjugation
Unconjugated
Type
Polyclonal Antibody
Applications
WB, IF
Purification Method
Affinity purification
Assay Type
Antibody
Concentration
1 mg/mL
Dilution
WB 1:500-1:2000 IF 1:50-1:200
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Storage Conditions
Store at -20°C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
18 kDa
Observed Molecular Weight
19 kDa
Host or Source
Rabbit
Isotype
IgG

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