Product Pathways - Translational Control
EDC4/Ge-1 Antibody #2548
PhosphoSitePlus® protein, site, and accession data: EDC4
| Applications | Reactivity | Sensitivity | MW (kDa) | Source |
|---|---|---|---|---|
| W IP IF-IC | H M Mk | Endogenous | 170 | Rabbit |
Applications Key:
W=Western Blotting
IP=Immunoprecipitation
IF-IC=Immunofluorescence (Immunocytochemistry)
Reactivity Key:
H=Human
M=Mouse
Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
Protocols
Specificity / Sensitivity
EDC4/Ge-1 Antibody detects endogenous levels of total EDC4/Ge-1 protein.
Source / Purification
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues near the amino terminus of human EDC4/Ge-1 protein. Antibodies are purified by protein A and peptide affinity chromatography.
Background
Enhancer of mRNA decapping 4 (EDC4) was originally identified as the autoantigen Ge-1 from a Sjögren's syndrome patient later diagnosed with primary biliary cirrhosis (1). EDC4 (also known as HEDLS) was later identified as an essential component of cytoplasmic P-bodies responsible for mRNA decapping and degradation (2). Identified EDC4 protein is found as a pair of isoforms generated by alternative splicing and contains several WD domains and a putative nuclear localization signal. EDC4 co-localizes with other P-body decapping proteins such as DCP1A, DCP2 and GW182 (2,3). Experimental evidence suggests that EDC4 may be involved in miRNA-mediated translation repression (4).
- Bloch, D.B. et al. (1994) Clin Immunol Immunopathol 72, 380-9.
- Yu, J.H. et al. (2005) RNA 11, 1795-802.
- Fenger-Grøn, M. et al. (2005) Mol Cell 20, 905-15.
- Brodersen, P. et al. (2008) Science 320, 1185-90.
Application References
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For Research Use Only. Not For Use In Diagnostic Procedures.