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WBSCR16

Williams-Beuren syndrome chromosome region 16

WBSCR16 encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants.

Gene Name: Williams-Beuren syndrome chromosome region 16
Synonyms: WBSCR16
Target Sequences: NM_030798 NP_110425.2 Q96I51

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Proteins (1)
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WBSCR16 Protein - 12.5% SDS-PAGE of human WBSCR16 stained with Coomassie Blue
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Wheat Germ Extract
GST
76.3 kDa
2 µg/$439
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If you do not find the reagent or information you require, please contact Customer.Support@LSBio.com to inquire about additional products in development.

PLEASE NOTE

For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).