XK (Human) Recombinant Protein
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Specification
Product Description
Human XK full-length ORF (AAH36019.1) recombinant protein without tag.
This product is belong to Proteoliposome (PL).Sequence
MKFPASVLASVFLFVAETTAALSLSSTYRSGGDRMWQALTLLFSLLPCALVQLTLLFVHRDLSRDRPLVLLLHLLQLGPLFRCFEVFCIYFQSGNNEEPYVSITKKRQMPKNGLSEEIEKEVGQAEGKLITHRSAFSRASVIQAFLGSAPQLTLQLYISVMQQDVTVGRSLLMTISLLSIVYGALRCNILAIKIKYDEYEVKVKPLAYVCIFLWRSFEIATRVVVLVLFTSVLKTWVVVIILINFFSLFLYPWILFWCSGSPFPENIEKALSRVGTTIVLCFLTLLYTGINMFCWSAVQLKIDSPDLISKSHNWYQLLVYYMIRFIENAILLLLWYLFKTDIYMYVCAPLLVLQLLIGYCTAILFMLVFYQFFHPCKKLFSSSVSEGFQRWLRCFCWACRQQKPCEPIGKEDLQSSRDRDETPSSSKTSPEPGQFLNAEDLCSA
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
77.3
Form
Liquid
Preparation Method
in vitro wheat germ expression system with proprietary liposome technology
Purification
None
Recommend Usage
Heating may cause protein aggregation. Please do not heat this product before electrophoresis.
Storage Buffer
25 mM Tris-HCl of pH8.0 containing 2% glycerol.
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
Antibody Production
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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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Interactome
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