Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1) Peptide
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- Target See all WHSC1 products
- WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
- Origin
- Human
- Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-WHSC1 antibody (Catalog #: ARP33489_P050). 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
- WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
- Synonyms
- WHSC1 Peptide, fc12c04 Peptide, wu:fc12c04 Peptide, wu:fi20c01 Peptide, si:rp71-77d7.2 Peptide, whs Peptide, nsd2 Peptide, trx5 Peptide, mmset Peptide, reiibp Peptide, MMSET Peptide, NSD2 Peptide, REIIBP Peptide, TRX5 Peptide, WHS Peptide, RGD1565590 Peptide, 5830445G22Rik Peptide, 9430010A17Rik Peptide, AW555663 Peptide, C130020C13Rik Peptide, D030027O06Rik Peptide, D930023B08Rik Peptide, Whsc1l Peptide, mKIAA1090 Peptide, nuclear receptor binding SET domain protein 2 Peptide, Wolf-Hirschhorn syndrome candidate 1 Peptide, NSD2 Peptide, nsd2 Peptide, WHSC1 Peptide, Nsd2 Peptide
- Background
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WHSC1 encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4.
Alias Symbols: WHS, NSD2, TRX5, MMSET, REIIBP
Protein Interaction Partner: HDAC1,HDAC2,KDM1A,SIN3A,SIN3B,WHSC1
Protein Size: 802 - Molecular Weight
- 88 kDa
- Gene ID
- 7468
- NCBI Accession
- NM_014919, NP_055734
- UniProt
- O96031
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