BIRC2 Antibody

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Product Specs

Buffer
Storage Buffer: PBS supplemented with 0.1% sodium azide, 50% glycerol, pH 7.3. Store at -20°C. Avoid freeze-thaw cycles.
Lead Time
Product dispatch typically occurs within 1-3 business days of order receipt. Delivery times may vary depending on the purchasing method and location. Please contact your local distributor for precise delivery estimates.
Synonyms
API 1 antibody; API1 antibody; Apoptosis inhibitor 1 antibody; Baculoviral IAP repeat containing 2 antibody; Baculoviral IAP repeat containing protein 2 antibody; Baculoviral IAP repeat-containing protein 2 antibody; BIRC 2 antibody; BIRC2 antibody; BIRC2_HUMAN antibody; C IAP1 antibody; C-IAP1 antibody; Cellular inhibitor of apoptosis 1 antibody; cellular inhibitor of apoptosis protein 1 antibody; cIAP 1 antibody; cIAP1 antibody; HIAP 2 antibody; HIAP-2 antibody; HIAP2 antibody; IAP 2 antibody; IAP homolog B antibody; IAP-2 antibody; IAP2 antibody; Inhibitor of apoptosis protein 2 antibody; MIHB antibody; NFR2 TRAF signalling complex protein antibody; RING finger protein 48 antibody; RNF 48 antibody; RNF48 antibody; TNFR2 TRAF signaling complex protein 2 antibody; TNFR2-TRAF-signaling complex protein 2 antibody
Target Names
Uniprot No.

Target Background

Function
The BIRC2 protein (also known as cIAP1) is a multifunctional protein with diverse regulatory roles. It influences caspase activity and apoptosis, modulates inflammatory signaling and immune responses, regulates mitogenic kinase signaling and cell proliferation, and impacts cell invasion and metastasis. Functioning as an E3 ubiquitin-protein ligase, it regulates NF-κB signaling, exhibiting both positive (canonical pathway) and negative (non-canonical pathway) effects. Its E3 ligase activity targets various proteins, including RIPK1, RIPK2, RIPK3, RIPK4, CASP3, CASP7, CASP8, TRAF2, DIABLO/SMAC, MAP3K14/NIK, MAP3K5/ASK1, IKBKG/NEMO, IKBKE, and MXD1/MAD1. cIAP1 also acts as an E3 ubiquitin ligase within the NEDD8 conjugation pathway, neddylating and inactivating effector caspases. It significantly regulates innate immune signaling through its interaction with pattern recognition receptors (PRRs), including Toll-like receptors (TLRs), Nod-like receptors (NLRs), and RIG-I-like receptors (RLRs). Crucially, cIAP1 protects cells from spontaneous ripoptosome formation (a caspase-dependent and -independent cell death mechanism) by ubiquitinating RIPK1 and CASP8. Furthermore, cIAP1 stimulates E2F1 transcriptional activity and plays a role in cell cycle modulation.
Gene References Into Functions

cIAP1's Role in Cellular Processes: Evidence from the Literature

  1. A study highlights distinct biological consequences of inhibiting versus activating cIAP1 E3 ligase activity, suggesting potential therapeutic strategies for targeting c-MYC in cancer by modulating cIAP1 activity. PMID: 30181285
  2. NAIP and cIAP expression patterns differ in polarized macrophages, suggesting a complex interplay in immune response. PMID: 29518103
  3. DMBT1, CRNDE, and c-IAP1 interaction within the PI3K-AKT pathway is implicated in gallbladder cancer carcinogenesis. PMID: 27637083
  4. cIAP1 regulates E2F1 stability and activity through non-degradative K63-polyubiquitination. PMID: 28542143
  5. High cIAP1 expression correlates with colorectal cancer. PMID: 27014915
  6. Cytoplasmic RARγ regulates RIP1-initiated cell death when cIAP activity is inhibited. PMID: 28871172
  7. High cIAP1 expression is associated with lung tumorigenesis. PMID: 27197231
  8. Molluscum contagiosum virus MC159 may competitively bind NEMO, preventing cIAP1-induced NEMO polyubiquitination. PMID: 28515292
  9. Baseline TNFα expression correlates with sensitivity to IAP antagonists. PMID: 27608596
  10. cIAP1-induced mitophagy leads to dysfunctional mitochondria and reduced ATP levels; cIAP1 ubiquitination is a critical regulator of this process. PMID: 27693792
  11. Overexpression of cIAP1 is associated with glioma. PMID: 26666816
  12. High cIAP1 expression is associated with triple-negative breast cancer. PMID: 26733177
  13. cIAP1/2 mediate BCL10 ubiquitination, essential for BCR-dependent NF-κB activity in DLBCL. PMID: 27070702
  14. AZD5582 induces apoptosis through Mcl-1 downregulation by targeting cIAP1 and XIAP in pancreatic cancer. PMID: 26314849
  15. Smac/DIABLO shows an inverse correlation with XIAP, cIAP-1, and cIAP-2. PMID: 25549803
  16. IRF-1 reduces NF-κB activity and suppresses TRAF2 and cIAP1 expression in breast cancer cells. PMID: 26011589
  17. cIAP1 is associated with tumor progression in human ovarian cancer. PMID: 26168135
  18. XIAP and cIAP1 activate NF-κB signaling, leading to Beclin 1 transcriptional activation and autophagy induction. PMID: 25669656
  19. cIAP1 and cIAP2 are potential therapeutic targets for preventing preterm birth. PMID: 25046208
  20. A20 downregulates cIAP1/2. PMID: 25911380
  21. GDC-0152 induces apoptosis in human leukemia through caspase-dependent mechanisms involving IAP downregulation and PI3K/Akt inhibition. PMID: 25273171
  22. IGF2BP1 is a critical translational regulator of cIAP1-mediated apoptotic resistance in rhabdomyosarcoma. PMID: 24704827
  23. Survivin affects cIAP1 stability, influencing cell sensitivity to YM155. PMID: 25635055
  24. cIAP1 and cIAP2 expression is increased in placenta from women with pre-existing maternal obesity and in response to pro-inflammatory cytokines. PMID: 25113061
  25. XIAP, cIAP1, and cIAP2 are critical regulators of cell death and survival, representing attractive cancer therapy targets. PMID: 24841289
  26. cIAP1 undergoes a conformational change during activation due to the dynamic nature of its closed form. PMID: 25383668, PMID: 25469840
  27. cIAP1 is involved in pancreatic beta cell survival during endoplasmic reticulum stress. PMID: 24559922
  28. cIAP1 regulates TNF-induced actin cytoskeleton reorganization through a cdc42-dependent pathway. PMID: 24276241
  29. ARC is regulated via BIRC2/MAP3K14 signaling and functions as a resistance factor to birinapant-induced leukemia cell death. PMID: 25079338
  30. EndoG interacts with cIAP1; IAPs ubiquitinate EndoG via K63 linkages without affecting EndoG levels, suggesting a regulatory role independent of degradation. PMID: 25139236
  31. cIAPs downregulate PACS-2, restraining TRAIL-induced killing of liver cancer cells. PMID: 24633224
  32. Selenite causes CYLD upregulation and cIAP downregulation, contributing to RIP1 degradation and apoptosis in colorectal tumor cells. PMID: 24577083
  33. XIAP and cIAP1 regulate the MEKK2/3-MEK5-ERK5 signaling module, influencing muscle cell differentiation. PMID: 24975362
  34. Higher cIAP1 expression is observed in ovarian endometriomas. PMID: 24382102
  35. Compounds sensitizing cancer cells to TRAIL effectively bind to XIAP and induce cIAP-1 and cIAP-2 degradation. PMID: 24194568
  36. Ceramide analogs sensitize metastatic colon and breast cancers to apoptosis, suppressing metastasis in vivo. PMID: 24422988
  37. Silencing of IAPs reduces TRAP-evoked RhoA activation. PMID: 24371121
  38. Cisplatin triggers proteasomal degradation of c-IAP1, c-IAP2, and XIAP in a ROS-dependent manner. PMID: 24425875
  39. Discovery of benzodiazepinone 36, a selective XIAP BIR2 inhibitor. PMID: 24093940
  40. A potent BIR2-selective inhibitor with in vivo pharmacokinetic properties potentiates apoptotic signaling. PMID: 24083782
  41. Palmitate does not decrease cIAP-1 and cIAP-2 mRNA expression. PMID: 24008361
  42. cIAP1 expression is decreased by Foxa2 silencing and increased by Foxa2 overexpression. PMID: 23275033
  43. BIRC2 and BIRC3 regulate JNK signaling, NF-κB, and fine-tune transcriptional responses. PMID: 23250032
  44. IAP antagonist-based cancer treatment may be compromised by osteoporosis. PMID: 23269702
  45. The BIRC2 3'UTR contains a cis-acting element affecting mRNA stability and protein expression. PMID: 23605047
  46. OTUB1 regulates NF-κB and MAPK signaling and TNF-dependent cell death by modulating c-IAP1 stability. PMID: 23524849
  47. A molecular mechanism for cIAP1 regulation in the NOD2 signaling pathway is described. PMID: 23109427
  48. c-IAP1 acts on PCSK9 secretion and lysosomal localization. PMID: 23085658
  49. IAP inhibitors and lexatumumab synergistically trigger apoptosis in RMS cells. PMID: 22927431
Database Links

HGNC: 590

OMIM: 601712

KEGG: hsa:329

STRING: 9606.ENSP00000227758

UniGene: Hs.696238

Protein Families
IAP family
Subcellular Location
Cytoplasm. Nucleus. Note=Agents that induce either the extrinsic or intrinsic apoptotic pathways promote its redistribution from the nuclear compartment to the cytoplasmic compartment. Associated with the midbody in telophase cells, and found diffusely in the nucleus of interphase cells.
Tissue Specificity
Present in many fetal and adult tissues. Mainly expressed in adult skeletal muscle, thymus, testis, ovary, and pancreas, low or absent in brain and peripheral blood leukocytes.

Q&A

Basic Research Questions

  • What is BIRC2 and what are its main functions in cellular processes?

    BIRC2 (Baculoviral IAP Repeat-Containing protein 2), also known as cIAP1, is a multi-functional protein belonging to the inhibitor of apoptosis (IAP) family. It is characterized by multiple baculoviral IAP repeats (BIR) and a RING finger domain . BIRC2 functions primarily as an E3 ubiquitin ligase and plays critical roles in:

    • Regulation of apoptosis through inhibition of caspase activation

    • Modulation of inflammatory signaling and immunity

    • Regulation of NF-κB signaling (both canonical and non-canonical pathways)

    • Cell proliferation and survival signaling

    • Cell invasion and metastasis processes

    Recent studies indicate that BIRC2 can interact with histone H3 in the nucleus and regulate genes involved in interferon and defense response signaling and cell-cycle regulation .

  • Which experimental applications are commonly supported by BIRC2 antibodies?

    Based on the analyzed data, BIRC2 antibodies support multiple research applications:

    ApplicationFrequency in ResearchCommon Protocols
    Western Blotting (WB)HighMost widely validated
    Immunohistochemistry (IHC)HighTissue section analysis
    ELISAModerateQuantitative detection
    Immunofluorescence (IF)ModerateCellular localization studies
    Immunocytochemistry (ICC)ModerateIn vitro cellular analysis
    Proximity Ligation Assay (PLA)LowProtein interaction studies
    Co-Immunoprecipitation (CoIP)LowProtein-protein interaction analysis

    When selecting BIRC2 antibodies, researchers should verify that the specific product has been validated for their application of interest .

  • How can I validate the specificity of my BIRC2 antibody?

    Validating antibody specificity is crucial for experimental reliability. Recommended validation approaches include:

    • Genetic controls: Use CRISPR-Cas9 knockout cell lines (as demonstrated in BIRC2 knockout studies in MCF7 breast cancer cells)

    • siRNA knockdown: Compare antibody signal between control and BIRC2 siRNA-treated samples (as performed in HCC cell lines)

    • Overexpression systems: Test antibody in cells transfected with BIRC2-overexpression plasmids versus controls

    • Western blot analysis: Verify a single band of appropriate molecular weight (~70 kDa for BIRC2)

    • Multiple antibody approach: Use antibodies targeting different epitopes of BIRC2 to confirm findings

    • Positive control selection: Use cell lines known to express BIRC2 (e.g., HeLa, Raji, NIH/3T3 cells)

  • What are the key differences between BIRC2 and BIRC3 expression and regulation?

    While BIRC2 and BIRC3 are related family members, research has identified important differences:

    CharacteristicBIRC2BIRC3
    Basal expressionReadily detected in unstimulated cells Lower basal expression
    Response to IL-1β/TNFModest enhancement (~2-5 fold) Strong induction (~20-50 fold)
    Response to glucocorticoidsGenerally unaffected Modestly increased
    Combined cytokine/glucocorticoidSometimes reduced Synergistic enhancement
    Protein stabilityMore stable baseline expression More dramatic regulation
    Response to IFNGLimited effect Variable enhancement at 24h
    Disease associationsMultiple cancers, RA, HIV-1 Often co-regulated with BIRC2

    These differences should be considered when designing experiments targeting specific IAP family members .

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