TBL2 Antibody (N-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| IHC-P, WB, E |
---|---|
Primary Accession | Q9Y4P3 |
Other Accession | NP_036585.1 |
Reactivity | Human |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 49798 Da |
Antigen Region | 43-72 aa |
Gene ID | 26608 |
---|---|
Other Names | Transducin beta-like protein 2, WS beta-transducin repeats protein, WS-betaTRP, Williams-Beuren syndrome chromosomal region 13 protein, TBL2, WBSCR13 |
Target/Specificity | This TBL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 43-72 amino acids from the N-terminal region of human TBL2. |
Dilution | WB~~1:1000 IHC-P~~1:10~50 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | TBL2 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | TBL2 |
---|---|
Synonyms | WBSCR13 |
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Provided below are standard protocols that you may find useful for product applications.
Background
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.
References
Hu, M., et al. Pharmacogenet. Genomics 20(10):634-637(2010)
Fontaine-Bisson, B., et al. Diabetologia 53(10):2155-2162(2010)
Keebler, M.E., et al. Circ Cardiovasc Genet 3(4):358-364(2010)
Hegele, R.A., et al. Hum. Mol. Genet. 18(21):4189-4194(2009)
Ruano, G., et al. Clin. Chim. Acta 400 (1-2), 48-55 (2009) :
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