Siva-1 Antibody #12532
Filter:
- WB
- IP
Supporting Data
REACTIVITY | H |
SENSITIVITY | Endogenous |
MW (kDa) | 19 |
SOURCE | Rabbit |
Application Key:
- WB-Western Blotting
- IP-Immunoprecipitation
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunoprecipitation | 1:50 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA and 50% glycerol. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
Siva-1 Antibody recognizes endogenous levels of total Siva-1 protein. This antibody does not cross-react with Siva-2. This antibody cross-reacts with a protein of unknown origin at ~70 kDa.
Species Reactivity:
Human
Source / Purification
Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Pro71 of human Siva-1 protein. Antibodies are purified by protein A and peptide affinity chromatography.
Background
First identified as a pro-apoptotic protein that binds the cytoplasmic tail of the TNF receptor superfamily member CD27 (1), Siva-1 also binds several other TNFR family members including glucocorticoid-induced tumor necrosis factor receptor (GITR) and OX40 (1-3), as well as anti-apoptotic Bcl-2 family members Bcl-xL and Bcl-2 (4,5). Siva-1 is composed of a central death domain homology region, a C-terminal box-B-like ring finger followed by a zinc finger-like domain, and a unique N-terminal amphipathic helical region (SAH) (1,4). Studies have demonstrated that Siva-1 has the ability to induce cell death via both the extrinsic and intrinsic apoptotic pathways (1-8). The SAH domain of Siva-1 is responsible for the inhibition of the pro-survival activities of Bcl-xL and Bcl-2, leading to caspase-mediated cell death (4,5,8). Siva-1 plays a role in T cell signaling and homeostasis by inhibiting NF-κB activity, also resulting in apoptotic cell death (7,9). An alternative splice variant of Siva-1, Siva-2, lacks part of the SAH and death domains and is less effective at inducing apoptosis (1,2,5,8). Studies in xenografts have shown that down-regulation of Siva-1 inhibits tumorigenesis in response to p53 activation (10). Down-regulation of Siva-1 may also play a role in tumor metastasis through its regulation of the epithelial-mesenchymal transition (EMT) and cell migration (11). Overexpression of Siva-1 is implicated in several pathological conditions including acute ischemic injury (12) and Coxsackievirus infection (13).
- Prasad, K.V. et al. (1997) Proc Natl Acad Sci U S A 94, 6346-51.
- Yoon, Y. et al. (1999) Oncogene 18, 7174-9.
- Spinicelli, S. et al. (2002) Cell Death Differ 9, 1382-4.
- Xue, L. et al. (2002) Proc Natl Acad Sci U S A 99, 6925-30.
- Chu, F. et al. (2004) Apoptosis 9, 83-95.
- Cao, C. et al. (2001) J Biol Chem 276, 11465-8.
- Gudi, R. et al. (2006) Oncogene 25, 3458-62.
- Py, B. et al. (2004) J Immunol 172, 4008-17.
- Hench, V.K. and Su, L. (2011) BMC Immunol 12, 54.
- Du, W. et al. (2009) Cell Death Differ 16, 1493-504.
- Li, N. et al. (2011) Proc Natl Acad Sci U S A 108, 12851-6.
- Padanilam, B.J. et al. (1998) Kidney Int 54, 1967-75.
- Henke, A. et al. (2000) J Virol 74, 4284-90.
限制使用
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For Research Use Only. Not For Use In Diagnostic Procedures.
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