cIAP2 Antibody (YA5260)
(Synonyms: AIP 1; AIP1; API 2; API2; API2; Apoptosis inhibitor 2; Baculoviral IAP repeat containing 3; Baculoviral IAP repeat containing protein 3; Baculoviral IAP repeat-containing protein 3; BIRC 3; BIRC3; BIRC3; BIRC3_HUMAN; C IAP2; C-IAP2; CIAP 2; CIAP 2; CIAP2; HAIP 1; HAIP1; HAIP1; HIAP 1; HIAP-1; HIAP1; IAP homolog C; IAP-1; Inhibitor of apoptosis protein 1; Inhibitor of apoptosis protein 1; MALT 2; MALT2; Mammalian IAP homolog C; MIHC; MIHC; RING finger protein 49; RNF49; TNFR2 TRAF signaling complex protein 1; TNFR2 TRAF signalling complex protein; TNFR2-TRAF-signaling complex protein 1.)cIAP2 Antibody (YA5260) is a Mouse-derived and non-conjugated monoclonal antibody, targeting to cIAP2.
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Host:
Mouse
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Application:
WB
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Reactivity :
Human, Monkey
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Formulation:
Supplied in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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|---|---|
| Dilution Ratio | 1:1000 |
Product Details
cIAP2 Antibody (YA5260) is a Mouse-derived and non-conjugated monoclonal antibody, targeting to cIAP2.
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Host Mouse
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Clonality Monoclonal
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Species ReactivityHuman, Monkey
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Observed Molecular WeightObserved band size: 72 kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
Purified recombinant human c-IAP2 protein fragments expressed in E.coli
affinity chromatography.
Non-conjugated
Unmodified
Product Properties
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Appearance
Solution
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Formulation
Supplied in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Envío
Shipping with blue ice.
Background
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Function
cIAP-2 (cellular inhibitor of apoptosis protein 2, encoded by BIRC3) is a member of the inhibitor of apoptosis protein (IAP) family that functions as a signaling regulator linking cell survival, inflammatory responses, and programmed cell death pathways[1][2]. Mechanistically, cIAP-2 acts as an E3 ubiquitin ligase within TNF receptor and pattern-recognition receptor signaling complexes, where it contributes to ubiquitination-dependent activation of NF-κB signaling and downstream transcriptional programs that support cellular adaptation to stress and immune stimulation[3][4]. Through cooperation with TRAF family proteins, cIAP-2 participates in the regulation of receptor-mediated signaling networks that control apoptosis, innate immunity, and inflammatory responses[3][5]. In disease settings, altered BIRC3 expression or mutation has been associated with hematologic malignancies and other cancers, highlighting the importance of cIAP-2 in tumor cell survival and therapy response[6][7]. Compared with the closely related isoform cIAP-1 (BIRC2), cIAP-2 displays distinct expression kinetics and regulatory patterns; cIAP-2 is strongly inducible by inflammatory cytokines through NF-κB-dependent mechanisms, whereas cIAP-1 is more constitutively expressed and is thought to support rapid signaling events[4]. This distinction suggests that cIAP-2 may contribute preferentially to sustained or later-phase signaling responses following inflammatory stimulation[4]. For experimental applications, cIAP-2 is widely investigated as a target of SMAC mimetics and other IAP-directed compounds that promote cIAP degradation or disrupt cIAP-associated signaling complexes, providing useful tools for studying NF-κB regulation, apoptosis sensitivity, and anticancer therapeutic mechanisms[2][8].
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Subcellular Localization
Cytoplasm; Nucleus
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Expression
Tissue_specificity:It is highly expressed in the fetal lungs and kidneys. In humans, it is primarily expressed in lymphoid tissues, including the spleen, thymus, and peripheral blood lymphocytes. -
Subunit
Interacts with PRSS25; interaction inhibits apoptotic suppressor activity. The BIR motifs region interacts with TNF receptor associated factors 1 and 2 (TRAF1 and TRAF2) to form a heteromeric complex, which is then recruited to the tumor necrosis factor receptor 2 (TNFR2). Interaction with TRAF2 is required for ubiquitination of IKBKE, degradation of NFKBIA and activation of NF-kappa-B. Interacts with RIP1, RIP2, RIP3, RIP4 and USP19
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SwissProt ID
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Synonyms
AIP 1; AIP1; API 2; API2; API2; Apoptosis inhibitor 2; Baculoviral IAP repeat containing 3; Baculoviral IAP repeat containing protein 3; Baculoviral IAP repeat-containing protein 3; BIRC 3; BIRC3; BIRC3; BIRC3_HUMAN; C IAP2; C-IAP2; CIAP 2; CIAP 2; CIAP2; HAIP 1; HAIP1; HAIP1; HIAP 1; HIAP-1; HIAP1; IAP homolog C; IAP-1; Inhibitor of apoptosis protein 1; Inhibitor of apoptosis protein 1; MALT 2; MALT2; Mammalian IAP homolog C; MIHC; MIHC; RING finger protein 49; RNF49; TNFR2 TRAF signaling complex protein 1; TNFR2 TRAF signalling complex protein; TNFR2-TRAF-signaling complex protein 1.
Documentación
[1]. Bertrand MJ, et al. Cellular inhibitors of apoptosis cIAP1 and cIAP2 are required for innate immunity signaling by the pattern recognition receptors NOD1 and NOD2. Immunity. 2009 Jun 19;30(6):789-801. [Content Brief]
[2]. Rabezanahary H, et al. Live virus neutralizing antibodies against pre and post Omicron strains in food and retail workers in Québec, Canada. Heliyon. 2024 May 21;10(10):e31026. [Content Brief]
[3]. Li Y, et al. Structure of natural killer cell receptor KLRG1 bound to E-cadherin reveals basis for MHC-independent missing self recognition. Immunity. 2009 Jul 17;31(1):35-46. [Content Brief]
[4]. Thorne A, et al. Differential regulation of BIRC2 and BIRC3 expression by inflammatory cytokines and glucocorticoids in pulmonary epithelial cells. PLoS One. 2023 Jun 8;18(6):e0286783. [Content Brief]
[5]. Lee MJ, et al. Time to HIV rebound after infusion of long-acting broadly neutralising antibodies 3BNC117-LS and 10-1074-LS and analytical treatment interruption (the RIO trial): a double-blind, randomised, placebo-controlled trial. Lancet HIV. 2026 May 27:S2352-3018(26)00059-7. [Content Brief]
[6]. Frazzi R. BIRC3 and BIRC5: multi-faceted inhibitors in cancer. Cell Biosci. 2021 Jan 7;11(1):8. doi: 10.1186/s13578-020-00521-0. PMID: 33413657; PMCID: PMC7792207. et al. BIRC3 and BIRC5: multi-faceted inhibitors in cancer. Cell Biosci. 2021 Jan 7;11(1):8. [Content Brief]
[7]. Yamato A, et al. Oncogenic activity of BIRC2 and BIRC3 mutants independent of nuclear factor-κB-activating potential. Cancer Sci. 2015 Sep;106(9):1137-42. [Content Brief]
[8]. Cossu F, et al. Computational and Experimental Characterization of NF023, A Candidate Anticancer Compound Inhibiting cIAP2/TRAF2 Assembly. J Chem Inf Model. 2020 Oct 26;60(10):5036-5044. [Content Brief]