Dsh-3 Antibody
Rabbit Monoclonal Antibody
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application ![]()
| WB, IHC |
---|---|
Primary Accession | Q92997 |
Reactivity | Human, Mouse, Rat |
Host | Rabbit |
Clonality | Monoclonal |
Clone Names | EP1991Y |
Calculated MW | 78055 Da |
Gene ID | 1857 |
Other Names | Segment polarity protein dishevelled homolog DVL-3, Dishevelled-3, DSH homolog 3, DVL3, KIAA0208 |
Target/Specificity | A synthetic peptide corresponding to residues near the C-terminus of human Dsh-3 was used as an immungen. |
Dilution | WB~~1:500 IHC~~1:100~250 |
Format | 50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | Dsh-3 Antibody is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | DVL3 |
---|---|
Synonyms | KIAA0208 |
Function | May play a role in the signal transduction pathway mediated by multiple Wnt genes. |
Cellular Location | Cytoplasm. |

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Provided below are standard protocols that you may find useful for product applications.
Background
The human DVL-3 gene encodes a predicted 716 amino acid protein which exhibits 98% amino acid identity with mouse Dsh-3 and 49% with Drosophila Dsh. Dsh-3 was mapped to 3q27. The expression of Dsh-3 mRNA was detected in 30 human cell lines and 2 primary cell cultures. Dsh-3 mRNA was detected in normal human breast tissues and tumors. Statistically, there was no difference in Dsh-3 mRNA level between normal breast tissues and tumors. In human colorectal samples, Dsh-3 was expressed equally in matched normal tissues, polyps and tumors. The data indicates that Dsh-3 is widely expressed in human cells and may have a widespread role in signal transduction (1). Results indicate that the human dishevelled genes constitute a multigene family and that Dsh 3 proteins are highly conserved among metazoans.
References
1. Bui TD, et al. Biochem Biophys Res Commun 239(2): 510-6, 1997.
2. Semenov MV, et al. Genomics 42(2):302-10, 1997

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