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WBSCR22 antibody (AA 1-281)

This Rabbit Polyclonal antibody specifically detects WBSCR22 in WB and IF. It exhibits reactivity toward Human.
Catalog No. ABIN6150175

Quick Overview for WBSCR22 antibody (AA 1-281) (ABIN6150175)

Target

See all WBSCR22 Antibodies
WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Reactivity

  • 29
  • 10
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 25
  • 4
Rabbit

Clonality

  • 27
  • 2
Polyclonal

Conjugate

  • 17
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This WBSCR22 antibody is un-conjugated

Application

  • 22
  • 9
  • 6
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 9
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-281

    Sequence

    MASRGRRPEH GGPPELFYDE TEARKYVRNS RMIDIQTRMA GRALELLYLP ENKPCYLLDI GCGTGLSGSY LSDEGHYWVG LDISPAMLDE AVDREIEGDL LLGDMGQGIP FKPGTFDGCI SISAVQWLCN ANKKSENPAK RLYCFFASLF SVLVRGSRAV LQLYPENSEQ LELITTQATK AGFSGGMVVD YPNSAKAKKF YLCLFSGPST FIPEGLSENQ DEVEPRESVF TNERFPLRMS RRGMVRKSRA WVLEKKERHR RQGREVRPDT QYTGRKRKPR F

    Cross-Reactivity

    Human, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-281 of human WBSCR22 (NP_059998.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

    Alternative Name

    WBSCR22

    Background

    This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.,BUD23,HASJ4442,HUSSY-3,MERM1,PP3381,WBMT,WBSCR22,Epigenetics & Nuclear Signaling,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,WBSCR22

    Molecular Weight

    24 kDa/31 kDa/33 kDa

    Gene ID

    114049

    UniProt

    O43709
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