Transducin (Beta)-Like 2 (TBL2) Peptide
TBL2
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all TBL2 products
- TBL2 (Transducin (Beta)-Like 2 (TBL2))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-TBL2 antibody (Catalog #: ARP53685_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
- TBL2 (Transducin (Beta)-Like 2 (TBL2))
- Synonyms
- wu:fa96f08 Peptide, tbl2 Peptide, MGC53692 Peptide, TBL2 Peptide, MGC79804 Peptide, MGC140759 Peptide, DKFZp469O1728 Peptide, WBSCR13 Peptide, WS-betaTRP Peptide, C76179 Peptide, WS-bTRP Peptide, transducin (beta)-like 2 Peptide, transducin (beta)-like 2 L homeolog Peptide, transducin beta like 2 Peptide, tbl2 Peptide, tbl2.L Peptide, TBL2 Peptide, Tbl2 Peptide
- Background
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TBL2 is a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. This gene encodes a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.
Alias Symbols: DKFZP43N024, MGC134739, WBSCR13, WS-betaTRP
Protein Interaction Partner: USP44
Protein Size: 447 - Molecular Weight
- 49 kDa
- Gene ID
- 26608
- NCBI Accession
- NM_012453, NP_036585
- UniProt
- Q9Y4P3
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