Product Name
Glycine cleavage system H protein, mitochondrial (GCSH), Recombinant Protein
Full Product Name
Recombinant Human Glycine cleavage system H protein, mitochondrial (GCSH)
Product Gene Name
GCSH recombinant protein
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Sequence Positions
49-173aa, Full Length of Mature Protein
Sequence
SVRKFTEKHE WVTTENGIGT VGISNFAQEA LGDVVYCSLP EVGTKLNKQD EFGALESVKA ASELYSPLSG EVTEINEALA ENPGLVNKSC YEDGWLIKMT LSNPSELDEL MSEEAYEKYI KSIEE
3D Structure
ModBase 3D Structure for P23434
Host
E Coli or Yeast or Baculovirus or Mammalian Cell
Purity/Purification
>85% (SDS-PAGE) (lot specific)
Form/Format
Liquid containing glycerol
Tag Information
This protein contains an N-terminal tag and may also contain a C-terminal tag. Tag types are determined by various factors including tag-protein stability, please inquire for tag information.
Sterility
Sterile filter available upon request.
Endotoxin
Low endotoxin available upon request.
Storage Buffer
Tris-based buffer, 50% glycerol
Preparation and Storage
Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80 degrees C. Store working aliquots at 4 degrees C for up to one week. Repeated freezing and thawing is not recommended.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of GCSH recombinant protein vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
NCBI/Uniprot data below describe general gene information for GCSH. It may not necessarily be applicable to this product.
NCBI Accession #
NP_004474.2
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NCBI GenBank Nucleotide #
NM_004483.4
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UniProt Primary Accession #
P23434
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UniProt Secondary Accession #
Q9H1E9[Other Products]
UniProt Related Accession #
P23434[Other Products]
Molecular Weight
18,885 Da
NCBI Official Full Name
glycine cleavage system H protein, mitochondrial
NCBI Official Synonym Full Names
glycine cleavage system protein H
NCBI Official Symbol
GCSH [Similar Products]
NCBI Official Synonym Symbols
GCE; NKH
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NCBI Protein Information
glycine cleavage system H protein, mitochondrial
UniProt Protein Name
Glycine cleavage system H protein, mitochondrial
UniProt Synonym Protein Names
Lipoic acid-containing protein
Protein Family
Glycine cleavage system H-like protein
UniProt Gene Name
GCSH [Similar Products]
NCBI Summary for GCSH
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.[provided by RefSeq, Jan 2010]
UniProt Comments for GCSH
The glycine cleavage system catalyzes the degradation of glycine. The H protein (GCSH) shuttles the methylamine group of glycine from the P protein (GLDC) to the T protein (GCST).
Research Articles on GCSH
1. Data indicate no mutation was found in glycine cleavage system protein-H (GCSH) and suggest that mutations in both glycine decarboxylase (GLDC) and aminomethyltransferase (AMT) are the main cause of glycine encephalopathy in Malaysian population.
Precautions
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Disclaimer
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