Overview

  • Product name
    Recombinant Human XK protein
  • Protein length
    Full length protein

Description

  • Nature
    Recombinant
  • Source
    Wheat germ
  • Amino Acid Sequence
    • Species
      Human
    • Sequence
      MKFPASVLASVFLFVAETTAALSLSSTYRSGGDRMWQALTLLFSLLPCAL VQLTLLFVHRDLSRDRPLVLLLHLLQLGPLFRCFEVFCIYFQSGNNEEPY VSITKKRQMPKNGLSEEIEKEVGQAEGKLITHRSAFSRASVIQAFLGSAP QLTLQLYISVMQQDVTVGRSLLMTISLLSIVYGALRCNILAIKIKYDEYE VKVKPLAYVCIFLWRSFEIATRVVVLVLFTSVLKTWVVVIILINFFSLFL YPWILFWCSGSPFPENIEKALSRVGTTIVLCFLTLLYTGINMFCWSAVQL KIDSPDLISKSHNWYQLLVYYMIRFIENAILLLLWYLFKTDIYMYVCAPL LVLQLLIGYCTAILFMLVFYQFFHPCKKLFSSSVSEGFQRWLRCFCWACR QQKPCEPIGKEDLQSSRDRDETPSSSKTSPEPGQFLNAEDLCSA
    • Amino acids
      1 to 444
    • Tags
      proprietary tag N-Terminus

Specifications

Our Abpromise guarantee covers the use of ab159821 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    ELISA

    Western blot

  • Form
    Liquid
  • Additional notes
    Protein concentration is above or equal to 0.05 mg/ml.
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.31% Glutathione, 0.79% Tris HCl

General Info

  • Alternative names
    • Kell complex 37 kDa component
    • Kx antigen
    • Membrane transport protein XK
    • XK
    • XK related protein 1
    • XK-related protein 1
    • XK_HUMAN
    • XKR1
    • XRG1
    see all
  • Function
    May be involved in sodium-dependent transport of neutral amino acids or oligopeptides.
  • Tissue specificity
    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.
  • Sequence similarities
    Belongs to the XK family.
  • Post-translational
    modifications
    Not glycosylated.
  • Cellular localization
    Membrane.
  • Information by UniProt

Images

  • ab159821 on a 12.5% SDS-PAGE stained with Coomassie Blue.

References

ab159821 has not yet been referenced specifically in any publications.

Customer reviews and Q&As

There are currently no Customer reviews or Questions for ab159821.
Please use the links above to contact us or submit feedback about this product.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

Sign up