Recombinant Human XK cell lysate
- Specification
- Gene Information
- Related Products
| 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; |
Products Types
Related Gene
XK
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
