WBSCR22 Antibody

Product: Alvimopan

WBSCR22 Antibody Summary

Immunogen
WBSCR22 (NP_059998.2, 1 a.a. ~ 281 a.a) full-length human protein.MASRGRRPEHGGPPELFYDETEARKYVRNSRMIDIQTRMAGRALELLYLPENKPCYLLDIGCGTGLSGSYLSDEGHYWVGLDISPAMLDEAVDREIEGDLLLGDMGQGIPFKPGTFDGCISISAVQWLCNANKKSENPAKRLYCFFASLFSVLVRGSRAVLQLYPENSEQLELITTQATKAGFSGGMVVDYPNSAKAKKFYLCLFSGPSTFIPEGLSENQDEVEPRESVFTNERFPLRMSRRGMVRKSRAWVLEK
Specificity
WBSCR22 – Williams Beuren syndrome chromosome region 22,
Clonality
Polyclonal
Host
Mouse
Gene
WBSCR22
Purity
Protein A purified
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Applications/Dilutions

Dilutions
  • Western Blot 1:500
  • ELISA
  • Immunocytochemistry/Immunofluorescence
Application Notes
Antibody reactive against recombinant protein with GST tag on ELISA and western blot and also on transfected lysate in western blot. GST tag alone is used as a negative control. It is also useful for immunofluoresence.

Reactivity Notes

Human.

Packaging, Storage & Formulations

Storage
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
Buffer
PBS (pH 7.4)
Preservative
No Preservative
Purity
Protein A purified

Notes

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for WBSCR22 Antibody

  • EC 2.1.1.-
  • FLJ44236
  • HASJ4442
  • HUSSY-3
  • MGC19709
  • MGC2022
  • MGC5140
  • PP3381
  • WBMT
  • Williams Beuren syndrome chromosome region 22 protein
  • Williams Beuren syndrome chromosome region 22
  • Williams-Beuren candidate region putative methyltransferase
  • Williams-Beuren syndrome chromosomal region 22 protein

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. [provided by RefSeq]

PMID: 26862589