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Recombinant Human XK protein
Full length protein
Amino Acid Sequence
MKFPASVLASVFLFVAETTAALSLSSTYRSGGDRMWQALTLLFSLLPCAL VQLTLLFVHRDLSRDRPLVLLLHLLQLGPLFRCFEVFCIYFQSGNNEEPY VSITKKRQMPKNGLSEEIEKEVGQAEGKLITHRSAFSRASVIQAFLGSAP QLTLQLYISVMQQDVTVGRSLLMTISLLSIVYGALRCNILAIKIKYDEYE VKVKPLAYVCIFLWRSFEIATRVVVLVLFTSVLKTWVVVIILINFFSLFL YPWILFWCSGSPFPENIEKALSRVGTTIVLCFLTLLYTGINMFCWSAVQL KIDSPDLISKSHNWYQLLVYYMIRFIENAILLLLWYLFKTDIYMYVCAPL LVLQLLIGYCTAILFMLVFYQFFHPCKKLFSSSVSEGFQRWLRCFCWACR QQKPCEPIGKEDLQSSRDRDETPSSSKTSPEPGQFLNAEDLCSA
1 to 444
proprietary tag N-Terminus
Our Abpromise guarantee covers the use of
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Stability and Storage
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
Constituents: 0.31% Glutathione, 0.79% Tris HCl
- Kell complex 37 kDa component
- Kx antigen
- Membrane transport protein XK
May be involved in sodium-dependent transport of neutral amino acids or oligopeptides.
High levels in skeletal muscle, heart, brain, and pancreas; low levels in placenta, lung, liver, and kidney.
Involvement in disease
Defects in XK are the cause of McLeod syndrome (MLS) [MIM:300842]. It is an X-linked multisystem disorder characterized by late onset abnormalities in the neuromuscular and hematopoietic systems.
Belongs to the XK family.
Information by UniProt
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"