Cdk5r1-flox Mouse
一般名
Cdk5r1-flox
製品ID
S-CKO-01675
背景情報
C57BL/6JCya
系統ID
CKOCMP-12569-Cdk5r1-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Cdk5r1-flox Mouse(カタログ番号S-CKO-01675)はサイアジェンから購入しました。」と引用してください。
製品タイプ
年齢
遺伝子型
性別
数量
標準的な配送方法では、少なくとも3匹のヘテロ接合体キャリアを保証しています。ホモ接合体キャリアや指定された性別の個体の繁殖サービスも利用可能です。
基本情報
系統名
Cdk5r1-flox
系統ID
CKOCMP-12569-Cdk5r1-B6J-VA
遺伝子名
製品ID
S-CKO-01675
遺伝子別名
p25, p35, Cdk5r, D11Bwg0379e
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 11
表現型
アプリケーション
--
さらに
系統詳細
EnsemblトランスクリプトID
ENSMUST00000053413
NCBIトランスクリプトID
NM_009871
ターゲット領域
Exon 1
有効領域の大きさ
~4.2 kb
遺伝子研究の概要
Cdk5r1, also known as cyclin-dependent kinase 5 regulatory subunit 1, encodes for p35, the main activator of Cyclin-dependent kinase 5 (CDK5). The active p35/CDK5 complex is involved in numerous aspects of brain development and function, and is associated with pathways like notch signaling [1,6]. It plays a crucial role in central nervous system development and neuronal migration [2].
In hepatocellular carcinoma (HCC), high Cdk5r1 expression is linked to adverse tumor status, new tumor events, clinical stage, topography, and worse survival outcomes, and can independently predict poor overall survival, disease-free interval, and progression-free interval [1]. In Schwann cells after sciatic nerve injury, overexpression of Cdk5r1 promotes cell proliferation, migration, and production of neurotrophic factors, and aids in nerve injury recovery through the CDK5/BDNF/TrkB pathway [2]. In Ewing's sarcoma cells, miR-152 suppresses cell proliferation by targeting Cdk5r1, and in multiple cancers including colorectal and breast malignancies, elevated Cdk5r1 expression is associated with poor prognosis, proliferation, and drug resistance [4,5]. In Alzheimer's disease, its down-regulation is related to specific subtypes and immune cell infiltration changes [3].
In conclusion, Cdk5r1 is essential for central nervous system development and neuronal migration. Studies, including those on various disease models, have shown its significance in cancer prognosis, peripheral nerve injury recovery, and neurodegenerative diseases. Understanding Cdk5r1 can provide insights into disease mechanisms and potential therapeutic targets.
References:
1. Zeng, Zhili, Cao, Zebiao, Zhang, Enxin, Huang, Haifu, Tang, Ying. . Elevated CDK5R1 predicts worse prognosis in hepatocellular carcinoma based on TCGA data. In Bioscience reports, 41, . doi:10.1042/BSR20203594. https://pubmed.ncbi.nlm.nih.gov/33346796/
2. Xia, Lei, Li, Peng, Bi, Wenchao, Yang, Ruize, Zhang, Yuelin. 2023. CDK5R1 promotes Schwann cell proliferation, migration, and production of neurotrophic factors via CDK5/BDNF/TrkB after sciatic nerve injury. In Neuroscience letters, 817, 137514. doi:10.1016/j.neulet.2023.137514. https://pubmed.ncbi.nlm.nih.gov/37848102/
3. Shao, Xu, Yang, Yanxian, Chen, Jieyun, Feng, Yu, Qin, Lina. 2022. Identification of Two CDK5R1-Related Subtypes and Characterization of Immune Infiltrates in Alzheimer's Disease Based on an Integrated Bioinformatics Analysis. In Computational and mathematical methods in medicine, 2022, 6766460. doi:10.1155/2022/6766460. https://pubmed.ncbi.nlm.nih.gov/36561735/
4. Kawano, Masanori, Tanaka, Kazuhiro, Itonaga, Ichiro, Kubota, Yuta, Tsumura, Hiroshi. 2023. Tumor-suppressive microRNA-152 inhibits the proliferation of Ewing's sarcoma cells by targeting CDK5R1. In Scientific reports, 13, 18546. doi:10.1038/s41598-023-45833-6. https://pubmed.ncbi.nlm.nih.gov/37899376/
5. Dastjerdi, Shaghayegh, Haghparast, Amin, Amroabadi, Jalal Mosayebi, Mahdevar, Mohammad, Ghaedi, Kamran. 2022. Elevated CDK5R1 expression associated with poor prognosis, proliferation, and drug resistance in colorectal and breast malignancies: CDK5R1 as an oncogene in cancers. In Chemico-biological interactions, 368, 110190. doi:10.1016/j.cbi.2022.110190. https://pubmed.ncbi.nlm.nih.gov/36162454/
6. Spreafico, Marco, Grillo, Barbara, Rusconi, Francesco, Battaglioli, Elena, Venturin, Marco. 2018. Multiple Layers of CDK5R1 Regulation in Alzheimer's Disease Implicate Long Non-Coding RNAs. In International journal of molecular sciences, 19, . doi:10.3390/ijms19072022. https://pubmed.ncbi.nlm.nih.gov/29997370/
品質管理基準
精子検査
凍結前の精子濃度を測定し、精子の生存能力の判定します。
凍結後の精子では、各バッチから1本の凍結保存された精子を選び出し、体外受精に使用します。
環境基準:
SPF対応地域:
グローバル由来:
Cyagenお問い合わせ
カスタムの動物モデルに関するご相談は、下記のフォームにご記入いただき、ご連絡いただくか見積もりをご依頼ください。
Cyagenはお客様のプライバシーを大変重視しています。当社の最新の製品や情報をお届けしたいと思っています。お客様の設定をご確認ください。
これらの配信はいつでも解除できます。配信停止方法およびデータ保護の詳細は プライバシーポリシー をご確認ください。
以下のボタンをクリックすることで、このフォームにご入力いただいた個人情報をCyagenが保存・処理し、ご要望のコンテンツを提供することに同意されたことになります。
