product summary
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company name :
MyBioSource
product type :
antibody
product name :
Rabbit anti-human X-linked Kx blood group (McLeod syndrome) polyclonal Antibody
catalog :
MBS712352
quantity :
0.05 mL
price :
375 USD
clonality :
polyclonal
host :
rabbit
conjugate :
nonconjugated
reactivity :
human, mouse, rat
application :
ELISA, immunohistochemistry, enzyme immunoassay
more info or order :
MyBioSource product webpage
product information
catalog number :
MBS712352
products type :
Antibody
products full name :
Rabbit anti-human X-linked Kx blood group (McLeod syndrome) polyclonal Antibody
products short name :
X-linked Kx blood group
products name syn :
X-linked Kx blood group (McLeod syndrome); XK; KX; X1k; XKR1
other names :
X-linked Kx blood group (McLeod syndrome); Membrane transport protein XK; membrane transport protein XK; Kx antigen; neurocanthocytosis; neuroacanthocytosis; XK-related protein 1; kell complex 37 kDa component; Kell blood group precursor (McLeod phenotype); XK, Kell blood group complex subunit (McLeod syndrome); X-linked Kx blood group; Kell complex 37 kDa component; Kx antigen; XK-related protein 1
other gene names :
XK; XK; KX; NA; NAC; X1k; XKR1; MCLDS; XKR1; XRG1
uniprot entry name :
XK_HUMAN
clonality :
Polyclonal
isotype :
IgG
host :
Rabbit
reactivity :
Human, Mouse, Rat
sequence length :
444
purity :
Antigen Affinity Purified
tested application :
ELISA (EIA), Immunohistochemistry (IHC)
other info1 :
Immunogen: Human XK
other info2 :
Storage Buffer: PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20 degree C, Avoid freeze / thaw cycles.
ncbi gi num :
23271200
ncbi acc num :
AAH36019.1
ncbi mol weight :
50,902 Da
ncbi summary :
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, Jul 2008]
uniprot summary :
XK: May be involved in sodium-dependent transport of neutral amino acids or oligopeptides. Defects in XK are the cause of McLeod syndrome (MLS). It is an X-linked multisystem disorder characterized by late onset abnormalities in the neuromuscular and hematopoietic systems. Belongs to the XK family. Protein type: Cell surface; Membrane protein, integral; Membrane protein, multi-pass. Chromosomal Location of Human Ortholog: Xp21.1. Cellular Component: integral to membrane. Molecular Function: protein binding; transporter activity. Biological Process: cellular calcium ion homeostasis; myelination; transport; amino acid transport; regulation of axon diameter; skeletal muscle fiber development; regulation of cell size. Disease: Mcleod Syndrome
size1 :
0.05 mL
price1 :
375 USD
size2 :
0.15 mL
price2 :
715
more info or order :
MyBioSource product webpage
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

"MyBioSource's number 1 vision is to be the world's number 1 quality reagents provider."

Our goal is to provide researchers, scientists and customers alike with a one-stop-shop for all of their reagents needs, whether it is monoclonal antibody, polyclonal antibody, recombinant protein, peptide, etc...

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