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Catalog No: OPCA60434
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OPCA60434
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Protein on Demand™ HINT1 Recombinant Protein (Human) (OPCA60434)

Datasheets/ManualsPrintable datasheet for OPCA60434
Product Info
Predicted Species ReactivityHuman
Product FormatLyophilized powder
ApplicationWB, ELISA
Additional InformationFor Research Use Only.
Sterile filtering available upon request.
Low endotoxin available upon request.
Reconstitution and StorageBriefly centrifuge lyophilized product prior to opening to bring the contents to the bottom. Please reconstitute protein to 0.1-1.0 mg/mL by adding deionized sterile water first, followed by addition of glycerol to a final concentration of 5-50%. Reconstituted product should be aliquoted for long-term storage at -20C/-80C. Our in house default final concentration of glycerol is 50% for reference. The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20C/-80C. The shelf life of lyophilized form is 12 months at -20C/-80C. Repeated freezing and thawing is not recommended. Store working aliquots at 4C for up to one week.
PurityGreater than 85% as determined by SDS-PAGE.
Protein SequenceADEIAKAQVARPGGDTIFGKIIRKEIPAKIIFEDDRCLAFHDISPQAPTHFLVIPKKHISQISVAEDDDESLLGHLMIVGKKCAADLGLNKGYRMVVNEGSDGGQSVYHVHLHVLGGRQMHWPPG
Storage BufferTris/PBS-based buffer, 6% Trehalose, pH 8.0
TagThis protein may contain a N-terminal tag or C-terminal tag based on protein stability requirements.
Gene SymbolHINT1
Gene Full Namehistidine triad nucleotide binding protein 1
Alias SymbolsHINT, NMAN, PKCI-1, PRKCNH1
NCBI Gene Id3094
Protein Namehistidine triad nucleotide-binding protein 1
Description of TargetThis gene encodes a protein that hydrolyzes purine nucleotide phosphoramidates substrates, including AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif. This gene is considered a tumor suppressor gene. In addition, mutations in this gene can cause autosomal recessive neuromyotonia and axonal neuropathy. There are several related pseudogenes on chromosome 7. Several transcript variants have been observed.
Uniprot IDP49773
Protein Accession #NP_005331.1
Nucleotide Accession #NM_005340.6
Protein Size (# AA)125
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