Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (C-Term) Peptide
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- Target See all WBSCR22 products
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- Protein Region
- C-Term
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Sequence
- GGAFERRGIR GHQTRRFPLR MSRRGMVRKS RAWVLEKKER HRRQGREVRP
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-WBSCR22 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- Synonyms
- MGC82375 Peptide, wbmt Peptide, pp3381 Peptide, hussy-3 Peptide, hasj4442 Peptide, zgc:162306 Peptide, HASJ4442 Peptide, HUSSY-3 Peptide, MERM1 Peptide, PP3381 Peptide, WBMT Peptide, 1110003N24Rik Peptide, Williams-Beuren syndrome chromosome region 22 Peptide, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog Peptide, BUD23, rRNA methyltransferase and ribosome maturation factor Peptide, williams Beuren syndrome chromosome region 22 Peptide, hypothetical protein Peptide, WBSCR22 Peptide, bud23.L Peptide, bud23 Peptide, CpipJ_CPIJ001394 Peptide, PAAG_00857 Peptide, MCYG_07273 Peptide, PGTG_07527 Peptide, PGTG_12505 Peptide, BUD23 Peptide, Bud23 Peptide
- Background
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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.
Alias Symbols: HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
Protein Size: 298 - Molecular Weight
- 32 kDa
- Gene ID
- 114049
- NCBI Accession
- NM_001202560, NP_001189489
- UniProt
- C9K060
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