XK X-linked Kx blood group Antibody

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Western Blot: XK X-linked Kx blood group Antibody [NBP1-69320] - This Anti-XK antibody was used in Western Blot of MCF7 tissue lysate at a concentration of 1ug/ml.

Product Details

Summary
Product Discontinued
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Order Details


    • Catalog Number
      NBP1-69320
    • Availability
      Product Discontinued

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XK X-linked Kx blood group Antibody Summary

Immunogen
Synthetic peptides corresponding to XK(X-linked Kx blood group (McLeod syndrome)) The peptide sequence was selected from the N terminal of XK. Peptide sequence LHLLQLGPLFRCFEVFCIYFQSGNNEEPYVSITKKRQMPKNGLSEEIEKE.
Clonality
Polyclonal
Host
Rabbit
Gene
XK
Purity
Immunogen affinity purified
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Applications/Dilutions

Dilutions
  • Western Blot 1:100-1:2000
Application Notes
This is a rabbit polyclonal antibody against XK and was validated on Western blot.
Theoretical MW
51 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
PBS & 2% Sucrose.
Preservative
No Preservative
Purity
Immunogen affinity purified

Notes

The addition of 50% glycerol is optional for those storing this antibody at -20C and not aliquoting smaller units. However, please note that glycerol may interrupt some downstream antibody applications and should be added with caution.

Alternate Names for XK X-linked Kx blood group Antibody

  • Kell blood group precursor (McLeod phenotype)
  • Kell complex 37 kDa component
  • Kx antigen
  • Kx
  • membrane transport protein XK
  • X1k
  • XK, Kell blood group complex subunit (McLeod syndrome)
  • XKR1XK-related protein 1
  • X-linked Kx blood group (McLeod syndrome)
  • XRG1

Background

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. XK has structural characteristics of prokaryotic and eukaryotic membrane transport proteins.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Publications for XK X-linked Kx blood group Antibody (NBP1-69320) (0)

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Bioinformatics

Gene Symbol XK
Uniprot