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X-linked Kx blood group (McLeod syndrome), Mouse, Polyclonal Antibody, Abnova™

Mouse polyclonal antibody raised against a full-length human XK protein.

Supplier:  Abnova Corporation H00007504B01

Catalog No. 89-006-454


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Description

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. [provided by RefSeq]

Sequence: MKFPASVLASVFLFVAETTAALSLSSTYRSGGDRMWQALTLLFSLLPCALVQLTLLFVHRDLSRDRPLVLLLHLLQLGPLFRCFEVFCIYFQSGNNEEPYVSITKKRQMPKNGLSEEIEKEVGQAEGKLITHRSAFSRASVIQAFLGSAPQLTLQLYISVMQQDVTVGRSLLMTISLLSIVYGALRCNILAIKIKYDEYEVKVKPLAYVCIFLWRSFEIATRVVVLVLFTSVLKTWVVVIILINFFSLFLYPWILFWCSGSPFPENIEKALSRVGTTIVLCFLTLLYTGINMFCWSAVQLKIDSPDLISKSHNWYQLLVYYMIRFIENAILLLLWYLFKTDIYMYVCAPLLVLQLLIGYCTAILFMLVFYQFFHPCKKLFSSSVSEGFQRWLRCFCWACRQQKPCEPIGKEDLQSSRDRDETPSSSKTSPEPGQFLNAEDLCSA
Specifications

Specifications

X-linked Kx blood group (McLeod syndrome)
Polyclonal
Mouse polyclonal antibody raised against a full-length human XK protein.
XK
KX/X1k/XKR1
Mouse
50 μL
Yes
7504
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
Western Blot
Unconjugated
No additive
BC036019.1
XK
XK (AAH36019.1, 1 a.a. ∼ 444 a.a) full-length human protein.
RUO
Primary
Human
Serum
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