XK (Human) Recombinant Protein (P01)
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More Files
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Specification
Product Description
Human XK full-length ORF ( AAH36019.1, 1 a.a. - 444 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MKFPASVLASVFLFVAETTAALSLSSTYRSGGDRMWQALTLLFSLLPCALVQLTLLFVHRDLSRDRPLVLLLHLLQLGPLFRCFEVFCIYFQSGNNEEPYVSITKKRQMPKNGLSEEIEKEVGQAEGKLITHRSAFSRASVIQAFLGSAPQLTLQLYISVMQQDVTVGRSLLMTISLLSIVYGALRCNILAIKIKYDEYEVKVKPLAYVCIFLWRSFEIATRVVVLVLFTSVLKTWVVVIILINFFSLFLYPWILFWCSGSPFPENIEKALSRVGTTIVLCFLTLLYTGINMFCWSAVQLKIDSPDLISKSHNWYQLLVYYMIRFIENAILLLLWYLFKTDIYMYVCAPLLVLQLLIGYCTAILFMLVFYQFFHPCKKLFSSSVSEGFQRWLRCFCWACRQQKPCEPIGKEDLQSSRDRDETPSSSKTSPEPGQFLNAEDLCSA
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
77.3
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 — XK
Entrez GeneID
7504GeneBank Accession#
BC036019.1Protein Accession#
AAH36019.1Gene Name
XK
Gene Alias
KX, X1k, XKR1
Gene Description
X-linked Kx blood group (McLeod syndrome)
Omim ID
314850Gene Ontology
HyperlinkGene Summary
This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq
Other Designations
Kell blood group precursor (McLeod phenotype)|Kx antigen|OTTHUMP00000031911|XK, Kell blood group complex subunit (McLeod syndrome)|XK-related protein 1|membrane transport protein XK
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