Logo
Homepage
Explore Our Models
My Cart
Contact
Subscribe
Models
Genetically Engineered Animals
Knockout Mice
Knockout Rats
Knockin Mice
Knockin Rats
Transgenic Mice
Transgenic Rats
Model Generation Techniques
Turboknockout<sup>®</sup> Gene Targeting
ES Cell Gene Targeting
Targeted Gene Editing
Regular Transgenic
PiggyBac Transgenesis
BAC Transgenic
Research Models
HUGO-GT™ Humanized Mice
Cre Mouse Lines
Humanized Target Gene Models
Metabolic Disease Models
Ophthalmic Disease Models
Neurological Disease Models
Autoimmune Disease Models
Immunodeficient Mouse Models
Humanized Immune System Mouse Models
Oncology & Immuno-oncology Models
Covid-19 Mouse Models
MouseAtlas Model Library
Knockout Cell Line Product Catalog
Tumor Cell Line Product Catalog
AAV Standard Product Catalog
Animal Supporting Services
Breeding Services
Cryopreservation & Recovery
Phenotyping Services
BAC Modification
Custom Cell Line Models
Induced Pluripotent Stem Cells (iPSCs)
Knockout Cell Lines
Knockin Cell Lines
Point Mutation Cell Lines
Overexpression Cell Lines
Virus Packaging
Adeno-associated Virus (AAV) Packaging
Lentivirus Packaging
Adenovirus Packaging
CRO Services
By Therapeutic Area
Oncology
Ophthalmology
Neuroscience
Metabolic & Cardiovascular Diseases
Autoimmune & Inflammatory
By Drug Type
AI-Powered AAV Discovery
Gene Therapy
Oligonucleotide Therapy
Antibody Therapy
Cell Immunotherapy
Resources
Promotion
Events & Webinars
Newsroom
Blogs & Insights
Resource Vault
Reference Databases
Peer-Reviewed Citations
Rare Disease Data Center
AbSeek
Cell iGeneEditor™ System
OriCell
Quality
Facility Overview
Animal Health & Welfare
Health Reports
About Us
Corporate Overview
Our Partners
Careers
Contact Us
Login
Request a Product Quote
Select products from our catalogs and submit your request. Our team will get back to you with detailed information.
Full Name
Email
Phone Number
Organization
Job Role
Country
Catalog Type
Product Name
Additional Comments
Cyagen values your privacy. We’d like to keep you informed about our latest offerings and insights. Your preferences:
You may unsubscribe from these communications at any time. See our Privacy Policy for details on opting out and data protection.
By clicking the button below, you consent to allow Cyagen to store and process the personal information submitted in this form to provide you the content requested.
C57BL/6JCya-Birc2em1flox/Cya
Common Name:
Birc2-flox
Product ID:
S-CKO-17938
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
Contact for Pricing
Basic Information
Strain Name
Birc2-flox
Strain ID
CKOCMP-11797-Birc2-B6J-VB
Gene Name
Birc2
Product ID
S-CKO-17938
Gene Alias
Api1; Api2; Birc3; C-IAP1; C330006D17Rik; HIAP1; HIAP2; IAP1; IAP2; MIAP1; MIAP2; MIHB; MIHC; RNF48; cIAP1; cIAP2; mcIAP1
Background
C57BL/6JCya
NCBI ID
11797
Modification
Conditional knockout
Chromosome
9
Phenotype
MGI:1197009
Document
Click here to download >>
Application
--
More
Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Birc2em1flox/Cya mice (Catalog S-CKO-17938) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000190341
NCBI RefSeq
NM_007465
Target Region
Exon 5~8
Size of Effective Region
~4.2 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Birc2, also known as baculoviral IAP repeat-containing 2, is a gene involved in regulating fundamental cell death and survival signaling pathways [5]. It can interact with other proteins, and its functions may relate to processes like immune response modulation and cell cycle regulation. The gene's role has been studied through various models to understand its biological importance in different physiological and pathological conditions.

Knockdown of BIRC2 in mouse melanoma or breast cancer cells increases the expression of chemokine CXCL9, impairs tumor growth by augmenting intratumoral activated CD8+ T cells and natural killer cells, and enhances the sensitivity of these tumors to anti-CTLA4 and/or anti-PD1 immune checkpoint blockade (ICB), indicating its role in cancer immune evasion and resistance to ICB [1]. In LPS-mediated C28/I2 cells (an in vitro rheumatoid arthritis (RA) cellular model), BIRC2 knockdown alleviates necroptosis, oxidative stress, and inflammation, and BIRC2 positively regulates TRADD expression, suggesting its potential as a novel target for RA treatment [2]. In hepatocellular carcinoma (HCC), BIRC2 promotes the ubiquitination-dependent degradation of NFκB-inducing kinase (NIK), inactivating the non-canonical NFκB signaling pathway, decreasing MHC-I expression, and protecting HCC cells from T cell-mediated cytotoxicity. Silencing or inhibiting BIRC2 increases the sensitivity of HCC cells to immune killing and improves the function of T cells, enhancing the efficacy of anti-PD-1 therapy [3]. In α7-HPV-related cervical squamous cell carcinoma (SCC), miR-143-3p targets BIRC2, and high BIRC2 expression is associated with poor outcomes. A combination of BIRC2-inhibitor LCL161 and topotecan shows synergistic effects on cancer cells and animal tumor models [4].

In conclusion, Birc2 plays crucial roles in multiple disease-related biological processes. Gene-knockout or knockdown models have revealed its functions in cancer immune evasion, rheumatoid arthritis progression, and HCC immune escape. Understanding Birc2's functions through these models provides potential therapeutic targets for cancer, rheumatoid arthritis, and other related diseases.

References:
1. Samanta, Debangshu, Huang, Tina Yi-Ting, Shah, Rima, Pan, Fan, Semenza, Gregg L. . BIRC2 Expression Impairs Anti-Cancer Immunity and Immunotherapy Efficacy. In Cell reports, 32, 108073. doi:10.1016/j.celrep.2020.108073. https://pubmed.ncbi.nlm.nih.gov/32846130/
2. Rao, Yanting, Xu, Shengjing, Lu, Ting, Liu, Manman, Zhang, Wei. . Downregulation of BIRC2 hinders the progression of rheumatoid arthritis through regulating TRADD. In Immunity, inflammation and disease, 11, e978. doi:10.1002/iid3.978. https://pubmed.ncbi.nlm.nih.gov/37904685/
3. Fu, Lingyi, Li, Shuo, Mei, Jie, Huang, Yuhua, Yun, Jingping. 2025. BIRC2 blockade facilitates immunotherapy of hepatocellular carcinoma. In Molecular cancer, 24, 113. doi:10.1186/s12943-025-02319-5. https://pubmed.ncbi.nlm.nih.gov/40223121/
4. Lin, Chiao-Yun, Wang, Chun-Chieh, Wu, Ren-Chin, Chao, Angel, Lai, Chyong-Huey. 2021. Inhibition of BIRC2 Sensitizes α7-HPV-Related Cervical Squamous Cell Carcinoma to Chemotherapy. In International journal of molecular sciences, 22, . doi:10.3390/ijms222011020. https://pubmed.ncbi.nlm.nih.gov/34681681/
5. Tencer, Adam H, Yu, Yucong, Causse, Sebastien Z, Shi, Xiaobing, Kutateladze, Tatiana G. 2023. Molecular basis for nuclear accumulation and targeting of the inhibitor of apoptosis BIRC2. In Nature structural & molecular biology, 30, 1265-1274. doi:10.1038/s41594-023-01044-1. https://pubmed.ncbi.nlm.nih.gov/37524969/
Quality Control Standard
Sperm Test

Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.

Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.

Environmental Standards:SPF
Available Region:Global
Source:Cyagen
Model Library
Model Library
Resources
Resources
Animal Quality
Animal Quality
Get Support
Get Support
Address:
2255 Martin Avenue, Suite E Santa Clara, CA 95050-2709, US
Tel:
800-921-8930 (8-6pm PST)
+1408-963-0306 (lnt’l)
Fax:
408-969-0338
Email:
animal-service@cyagen.com
service@cyagen.us
CRO Services
OncologyOphthalmologyNeuroscienceMetabolic & CardiovascularAutoimmune & InflammatoryGene TherapyAntibody Therapy
About Us
Corporate OverviewOur PartnersCareersContact Us
Social Media
Disclaimer: Pricing and availability of our products and services vary by region. Listed prices are applicable to the specific countries. Please contact us for more information.
Copyright © 2025 Cyagen. All rights reserved.
Privacy Policy
Site Map
Stay Updated with the Latest from Cyagen
Get the latest news on our research models, CRO services, scientific resources, and special offers—tailored to your research needs and delivered straight to your inbox.
Full Name
Email
Organization
Country
Areas of Interest