Recombinant Human AMT protein (ab202602)
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Description
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Product name
Recombinant Human AMT protein -
Purity
> 90 % SDS-PAGE.
ab202602 was purified using conventional chromatography techniques. -
Expression system
Escherichia coli -
Accession
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Protein length
Full length protein -
Animal free
No -
Nature
Recombinant -
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Species
Human -
Sequence
MGSSHHHHHHSSGLVPRGSHMGSAQEVLRRTPLYDFHLAHGGKMVAFAGW SLPVQYRDSHTDSHLHTRQHCSLFDVSHMLQTKILGSDRVKLMESLVVGD IAELRPNQGTLSLFTNEAGGILDDLIVTNTSEGHLYVVSNAGCWEKDLAL MQDKVRELQNQGRDVGLEVLDNALLALQGPTAAQVLQAGVADDLRKLPFM TSAVMEVFGVSGCRVTRCGYTGEDGVEISVPVAGAVHLATAILKNPEVKL AGLAARDSLRLEAGLCLYGNDIDEHTTPVEGSLSWTLGKRRRAAMDFPGA KVIVPQLKGRVQRRRVGLMCEGAPMRAHSPILNMEGTKIGTVTSGCPSPS LKKNVAMGYVPCEYSRPGTMLLVEVRRKQQMAVVSKMPFVPTNYYTLK -
Predicted molecular weight
43 kDa including tags -
Amino acids
29 to 403 -
Tags
His tag N-Terminus -
Additional sequence information
This product is for the mature full length protein from aa 29 to 403. The signal peptide is not included. NP_000472
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Associated products
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Related Products
Specifications
Our Abpromise guarantee covers the use of ab202602 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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Applications
Mass Spectrometry
SDS-PAGE
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Mass spectrometry
MALDI-TOF -
Form
Liquid -
Concentration information loading...
Preparation and Storage
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Stability and Storage
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Constituents: 30% Glycerol, 0.02% DTT, 69% PBS
General Info
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Alternative names
- Aminomethyltransferase
- Aminomethyltransferase (glycine cleavage system protein T)
- AMT
see all -
Function
The glycine cleavage system catalyzes the degradation of glycine. -
Involvement in disease
Non-ketotic hyperglycinemia -
Sequence similarities
Belongs to the GcvT family. -
Cellular localization
Mitochondrion. - Information by UniProt
Images
Datasheets and documents
References
ab202602 has not yet been referenced specifically in any publications.