Overview

Description

  • Nature
    Recombinant
  • Source
    Wheat germ
  • Amino Acid Sequence
    • Species
      Human
    • Sequence
      MADQGEKENPMRELRIRKLCLNICVGESGDRLTRAAKVLEQLTGQTPVFS KARYTVRSFGIRRNEKIAVHCTVRGAKAEEILEKGLKVREYELRKNNFSD TGNFGFGIQEHIDLGIKYDPSIGIYGLDFYVVLGRPGFSIADKKRRTGCI GAKHRISKEEAMRWFQQKYDGIILPGK
    • Amino acids
      1 to 177
    • Tags
      proprietary tag N-Terminus

Specifications

Our Abpromise guarantee covers the use of ab159381 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
    • 60S ribosomal protein L11
    • Cell growth inhibiting protein 34
    • Cell growth inhibiting protein34
    • CLL associated antigen KW 12
    • CLL associated antigen KW12
    • CLL-associated antigen KW-12
    • DBA 7
    • DBA7
    • GIG 34
    • GIG34
    • L11
    • Ribosomal protein L11
    • RL11_HUMAN
    • RPL 11
    • Rpl11
    see all
  • Function
    Binds to 5S ribosomal RNA (By similarity). Required for rRNA maturation and formation of the 60S ribosomal subunits. Promotes nucleolar location of PML.
  • Involvement in disease
    Defects in RPL11 are the cause of Diamond-Blackfan anemia type 7 (DBA7) [MIM:612562]. DBA7 is a form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies.
  • Sequence similarities
    Belongs to the ribosomal protein L5P family.
  • Cellular localization
    Nucleus > nucleolus.
  • Information by UniProt

Images

  • ab159381 on a 12.5% SDS-PAGE stained with Coomassie Blue.

References

ab159381 has not yet been referenced specifically in any publications.

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

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