SLC23A2 (Human) Recombinant Protein (P01)
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More Files
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Specification
Product Description
Human SLC23A2 full-length ORF ( AAH13112.1, 1 a.a. - 425 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MMGIGKNTTSKSMEAGSSTEGKYEDEAKHPAFFTLPVVINGGATSSGEQDNEDTELMAIYTTENGIAEKSSLAETLDSTGSLDPQRSDMIYTIEDVPPWYLCIFLGLQHYLTCFSGTIAVPFLLADAMCVGYDQWATSQLIGTIFFCVGITTLLQTTFGCRLPLFQASAFAFLAPARAILSLDKWKCNTTDVSVANGTAELLHTEHIWYPRIREIQGAIIMSSLIEVVIGLLGLPGALLKYIGPLTITPTVALIGLSGFQAAGERAGKHWGIAMLTIFLVLLFSQYARNVKFPLPIYKSKKGWTAYKLQLFKMFPIILAILVSWLLCFIFTVTDVFPPDSTKYGFYARTDARQGVLLVAPWFKVPYPFQWGLPTVSAAGVIGMLSAVVASIIESIGDYYACARLSCAPPPPIHAINRYVPEKTSS
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
72.8
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — SLC23A2
Entrez GeneID
9962GeneBank Accession#
BC013112.2Protein Accession#
AAH13112.1Gene Name
SLC23A2
Gene Alias
KIAA0238, NBTL1, SLC23A1, SVCT2, YSPL2
Gene Description
solute carrier family 23 (nucleobase transporters), member 2
Omim ID
603791Gene Ontology
HyperlinkGene Summary
The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1. [provided by RefSeq
Other Designations
Na(+)/L-ascorbic acid transporter 2|OTTHUMP00000030173|OTTHUMP00000030174|sodium-dependent vitamin C transporter-2|solute carrier family 23 (nucleobase transporters), member 1|yolk sac permease-like molecule 2
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Interactome
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Disease
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