Ikbkb-flox Mouse
Common Name
Ikbkb-flox
제품 ID
S-CKO-03072
Backgroud
C57BL/6JCya
품종 계통계통 ID
CKOCMP-16150-Ikbkb-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Ikbkb-flox Mouse (카탈로그 번호 S-CKO-03072)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
기본 정보
품종 계통
Ikbkb-flox
품종 계통계통 ID
CKOCMP-16150-Ikbkb-B6J-VA
유전자명
제품 ID
S-CKO-03072
유전자 별칭
IKK2, IKK-2, IKK[b], IKKbeta, IKK-beta
배경
C57BL/6JCya
NCBI ID
변형 내용
Conditional knockout
염색체
Chr 8
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000063401
NCBI 전사체 ID
NM_010546
타겟 영역
Exon 4
유효 영역 크기
~1.0 kb
유전자 연구 개요
Ikbkb, also known as IKKβ (IkappaB kinase beta) or IKK2, is a key molecule in the signaling pathway to the transcription factor NF-κB. Its kinase activity phosphorylates IkappaB molecules, leading to their ubiquitination and proteasomal degradation, and subsequent release and activation of NF-κB. Many signaling pathways that activate NF-κB converge at the level of Ikbkb. NF-κB has diverse functions in regulating the immune system, cellular differentiation, survival, and proliferation. Ikbkb is thus crucial in acute and chronic inflammation, which is associated with various diseases, and also in cancer where NF-κB can act as a survival factor for malignant cells [7].
In Huntington's disease, Ikbkb can regulate endogenous S13 huntingtin phosphorylation via a non-canonical interferon regulatory factor3-mediated IKK pathway, reducing mutant huntingtin aggregation [1]. In a male infant with a heterozygous gain-of-function (GOF) Ikbkb variant, it was associated with autoimmunity and autoinflammation, showing increased basal levels of phosphorylation of IKKα/β and p65, and higher degradation of IkBα in transduced Jurkat cells [2]. In spinal nerve ligation (SNL) rats, delivering Ikbkb small interfering RNA (siRNA)-encapsulated poly (lactic-co-glycolic acid) (PLGA) nanoparticles reduced neuropathic pain by inhibiting microglial activation [3]. In clear cell renal cell carcinoma (ccRCC), decreased Ikbkb expression was observed, and patients with upregulated Ikbkb protein expression had higher nuclear grade tumors and shorter survival [4]. In hepatocellular carcinoma (HCC), IKKβ phosphorylated and stabilized USP30, promoting lipogenesis and tumorigenesis [5]. In gliomagenesis, α-ketoglutarate-produced by GDH1 under low glucose-directly binds to and activates IKKβ and NF-κB signaling, promoting glucose uptake and tumor cell survival [6]. In osteoarthritis, decreased miR-214-3p activates the NF-κB signaling pathway and aggravates OA development through targeting Ikbkb [8].
In conclusion, Ikbkb is essential in the NF-κB signaling pathway and has a significant impact on various biological processes and disease conditions such as neurodegenerative diseases, autoimmune and autoinflammatory disorders, neuropathic pain, cancer, and osteoarthritis. Studies on Ikbkb, especially through functional models, help in understanding disease mechanisms and may provide potential therapeutic targets.
References:
1. Cariulo, Cristina, Martufi, Paola, Verani, Margherita, Petricca, Lara, Caricasole, Andrea. 2023. IKBKB reduces huntingtin aggregation by phosphorylating serine 13 via a non-canonical IKK pathway. In Life science alliance, 6, . doi:10.26508/lsa.202302006. https://pubmed.ncbi.nlm.nih.gov/37553253/
2. Sacco, Keith, Kuehn, Hye Sun, Kawai, Tomoki, Rosenzweig, Sergio D, Keller, Michael D. 2022. A Heterozygous Gain-of-Function Variant in IKBKB Associated with Autoimmunity and Autoinflammation. In Journal of clinical immunology, 43, 512-520. doi:10.1007/s10875-022-01395-2. https://pubmed.ncbi.nlm.nih.gov/36378426/
3. Lee, Seounghun, Shin, Hyo-Jung, Noh, Chan, Lee, Won-Hyung, Kim, Yoon-Hee. 2021. IKBKB siRNA-Encapsulated Poly (Lactic-co-Glycolic Acid) Nanoparticles Diminish Neuropathic Pain by Inhibiting Microglial Activation. In International journal of molecular sciences, 22, . doi:10.3390/ijms22115657. https://pubmed.ncbi.nlm.nih.gov/34073390/
4. Krazinski, Bartlomiej E, Kowalczyk, Anna E, Sliwinska-Jewsiewicka, Agnieszka, Kmiec, Zbigniew, Kiewisz, Jolanta. 2018. IKBKB expression in clear cell renal cell carcinoma is associated with tumor grade and patient outcomes. In Oncology reports, 41, 1189-1197. doi:10.3892/or.2018.6872. https://pubmed.ncbi.nlm.nih.gov/30483769/
5. Gu, Li, Zhu, Yahui, Lin, Xi, Prochownik, Edward V, Li, Youjun. 2020. The IKKβ-USP30-ACLY Axis Controls Lipogenesis and Tumorigenesis. In Hepatology (Baltimore, Md.), 73, 160-174. doi:10.1002/hep.31249. https://pubmed.ncbi.nlm.nih.gov/32221968/
6. Wang, Xiongjun, Liu, Ruilong, Qu, Xiujuan, Li, Guohui, Yang, Weiwei. 2019. α-Ketoglutarate-Activated NF-κB Signaling Promotes Compensatory Glucose Uptake and Brain Tumor Development. In Molecular cell, 76, 148-162.e7. doi:10.1016/j.molcel.2019.07.007. https://pubmed.ncbi.nlm.nih.gov/31447391/
7. Schmid, Johannes A, Birbach, Andreas. 2008. IkappaB kinase beta (IKKbeta/IKK2/IKBKB)--a key molecule in signaling to the transcription factor NF-kappaB. In Cytokine & growth factor reviews, 19, 157-65. doi:10.1016/j.cytogfr.2008.01.006. https://pubmed.ncbi.nlm.nih.gov/18308615/
8. Cao, Yumei, Tang, Su'an, Nie, Xiaoyu, Zhu, Zhaohua, Ding, Changhai. 2021. Decreased miR-214-3p activates NF-κB pathway and aggravates osteoarthritis progression. In EBioMedicine, 65, 103283. doi:10.1016/j.ebiom.2021.103283. https://pubmed.ncbi.nlm.nih.gov/33714889/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
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