"XK" Related Products

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Recombinant Human XK cell lysate

Cat.No.: XK-1936HCL
Description: 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.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: XK X-linked Kx blood group (McLeod syndrome) [ Homo sapiens ]
Official Symbol: XK
Synonyms: XK; X-linked Kx blood group (McLeod syndrome); Kell blood group precursor (McLeod phenotype) , XK, Kell blood group complex subunit (McLeod syndrome); membrane transport protein XK; Kx; Kx antigen; X1k; XKR1; XK-related protein 1; kell complex 37 kDa component; Kell blood group precursor (McLeod phenotype); XK, Kell blood group complex subunit (McLeod syndrome); KX; MCLDS;
Gene ID: 7504
mRNA Refseq: NM_021083
Protein Refseq: NP_066569
MIM: 314850
UniProt ID: P51811
Chromosome Location: Xp21.1
Function: protein binding; transporter activity;

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