Recombinant Human XK cell lysate

• Cat.No.: XK-1936HCL

Specification

• Species: Human
• Tag: Non
• 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.
• 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 Information

• 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