Kdr-flox Mouse
一般名
Kdr-flox
製品ID
S-CKO-03246
背景情報
C57BL/6JCya
系統ID
CKOCMP-16542-Kdr-B6J-VA
状況
このマウス系統を論文で使用する場合は、「Kdr-flox Mouse(カタログ番号S-CKO-03246)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
Kdr-flox
系統ID
CKOCMP-16542-Kdr-B6J-VA
遺伝子名
製品ID
S-CKO-03246
遺伝子別名
orv, Flk1, Ly73, Flk-1, Krd-1, VEGFR2, VEGFR-2, sVEGFR-2, 6130401C07
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 5
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
ENSMUST00000113516
NCBIトランスクリプトID
NM_010612
ターゲット領域
Exon 3
有効領域の大きさ
~0.9 kb
遺伝子研究の概要
Kdr, also known as Kinase insert Domain containing Receptor or Vascular Endothelial Growth Factor Receptor (VEGFR-2), is involved in endothelial dysfunction and plays a role in many biological processes. It is associated with pathways related to angiogenesis, as seen in its influence on tumor neovascularization in colorectal cancer [5]. In the context of insects, kdr-type resistance is due to mutations in the para-homologous sodium channel gene, causing insensitivity of the nervous system to pyrethroids and DDT [3].
In houseflies, kdr-type alleles such as kdr (L1014F), kdr-his (L1014H), super-kdr (M918T + L1014F), type N (D600N + M918T + L1014F), and 1B (T929I + L1014F) have led to resistance against pyrethroids. High levels of resistance are associated with the L1014F mutation in North America, Europe, and Asia [1]. In Aedes aegypti mosquitoes in Brazil, kdr mutations (Val1016Ile and Phe1534Cys) have rapidly spread and increased in frequency, and a 'kdr index' was introduced to analyze spatial patterns [6]. In Aedes albopictus, kdr mutations associated with resistance to DDT and pyrethroids were first evidenced in 2011 and have since been reported in various regions worldwide [7]. In house flies in Abu Dhabi, UAE, the kdr allele was found in most sampling locations, and in addition to the L1014F mutation, L1014H and T929I mutations were detected [8].
In conclusion, Kdr has diverse functions. In insects, kdr-related mutations are crucial in conferring resistance to insecticides, which has implications for pest control strategies. In human-related research, Kdr is associated with various diseases. Its role in endothelial dysfunction, angiogenesis, and its influence on disease severity and drug-induced hepatotoxicity, as well as its potential as a predictor for immunotherapy in pan-cancer, highlight its importance in understanding disease mechanisms and developing treatment strategies [1,2,4,5,9].
References:
1. Roca-Acevedo, Gonzalo, Boscaro, Ivana, Toloza, Ariel Ceferino. 2022. Global Pattern of kdr-Type Alleles in Musca domestica (L.). In Current tropical medicine reports, 10, 1-10. doi:10.1007/s40475-022-00281-6. https://pubmed.ncbi.nlm.nih.gov/36569791/
2. Singh, HariOm, Samani, Dharmesh, Jadhav, Sushama. 2021. KDR polymorphism (1192G/A, 1719A/T) and modulation of ARV drug-induced hepatotoxicity. In Microbial pathogenesis, 161, 105243. doi:10.1016/j.micpath.2021.105243. https://pubmed.ncbi.nlm.nih.gov/34656700/
3. Scott, J G, Dong, K. . kdr-Type resistance in insects with special reference to the German cockroach, Blattella germanica. In Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology, 109, 191-8. doi:. https://pubmed.ncbi.nlm.nih.gov/7553340/
4. Paradowska-Gorycka, Agnieszka, Stypinska, Barbara, Pawlik, Andrzej, Manczak, Malgorzata, Olesinska, Marzena. 2019. KDR (VEGFR2) Genetic Variants and Serum Levels in Patients with Rheumatoid Arthritis. In Biomolecules, 9, . doi:10.3390/biom9080355. https://pubmed.ncbi.nlm.nih.gov/31405022/
5. Mohammad Rezaei, Fatemeh, Hashemzadeh, Shahryar, Ravanbakhsh Gavgani, Reyhaneh, Taheri, Mohammad, Sakhinia, Ebrahim. . Dysregulated KDR and FLT1 Gene Expression in Colorectal Cancer Patients. In Reports of biochemistry & molecular biology, 8, 244-252. doi:. https://pubmed.ncbi.nlm.nih.gov/32274396/
6. Melo Costa, Monique, Campos, Kauara Brito, Brito, Luiz Paulo, Lima, José Bento Pereira, Martins, Ademir Jesus. 2020. Kdr genotyping in Aedes aegypti from Brazil on a nation-wide scale from 2017 to 2018. In Scientific reports, 10, 13267. doi:10.1038/s41598-020-70029-7. https://pubmed.ncbi.nlm.nih.gov/32764661/
7. Auteri, Michelangelo, La Russa, Francesco, Blanda, Valeria, Torina, Alessandra. 2018. Insecticide Resistance Associated with kdr Mutations in Aedes albopictus: An Update on Worldwide Evidences. In BioMed research international, 2018, 3098575. doi:10.1155/2018/3098575. https://pubmed.ncbi.nlm.nih.gov/30175124/
8. Hamdan, Mohamad, Kamalanathan, Tamilarasan, Iqbal, Asim, Ali, Amgd Sayed, Al-Deeb, Mohammad Ali. 2024. kdr mutations and deltamethrin resistance in house flies in Abu Dhabi, UAE. In Parasites & vectors, 17, 47. doi:10.1186/s13071-024-06128-5. https://pubmed.ncbi.nlm.nih.gov/38302967/
9. Cui, Yanan, Zhang, Pengpeng, Liang, Xiao, Zhang, Fang, Guo, Renhua. 2022. Association of KDR mutation with better clinical outcomes in pan-cancer for immune checkpoint inhibitors. In American journal of cancer research, 12, 1766-1783. doi:. https://pubmed.ncbi.nlm.nih.gov/35530271/
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。
