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重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白

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  • 产品名称:重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白
  • 产品型号:rHup16-INK4a-TAT
  • 产品展商:KALANG
  • 产品文档:无相关文档
  • 发布时间:2016-12-21
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简单介绍
重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白与其它公司提供的重组蛋白不同,rHup16-INK4a-TAT蛋白产品为采用CFS的无细胞麦胚蛋白合成系统表达出来的重组蛋白,可表达出对细胞有毒性、易被蛋白酶降解的蛋白;并获得具有良好的可溶性,并有翻译后修饰、从而部分具有功能的蛋白.同时独有的全自动蛋白纯化技术则简便高效,将蛋白纯化过程中对蛋白的损伤降低到*小程度.重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白(全长序列)产品可用于Western Blot验证、抗体制备、蛋白检测、ELISA等试验中.
产品描述

重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白

Synonyms CDK4I, MTS-1, p16INK4A
Species Human
Source Escherichia coli.
Molecular Weight Approximately18.0 kDa, a single non-glycosylated polypeptide chain containing 167 amino acids.
Quantity 5µg/25µg/1000µg
AA Sequence 重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白EPAAGSSMEP SADWLATAAA RGRVEEVRAL LEAGALPNAP NSYGRRPIQV MMMGSARVAE LLLLHGAEPN CADPATLTRP VHDAAREGFL DTLVVLHRAG ARLDVRDAWG RLPVDLAEEL GHRDVARYLR AAAGGTRGSN HARIDAAEGP SDIPDGYGRK KRRQRRR
Purity > 95 % by SDS-PAGE and HPLC analyses.
Biological Activity Data is not available.
Physical Appearance 重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白Sterile Filtered White lyophilized (freeze-dried) powder.
Formulation Lyophilized from a 0.2 µm filtered concentrated solution in 2 × PBS, pH 7.0.
Endotoxin Less than 1 EU/µg of rHuP16-INK4a-TAT as determined by LAL method.
Reconstitution 重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Reconstitute in sterile distilled water or aqueous buffer containing 0.1 % BSA to a concentration of 0.1-1.0 mg/ml. Stock solutions should be apportioned into working aliquots and stored at ≤ -20 °C. Further dilutions should be made in appropriate buffered solutions.
Storage This lyophilized preparation is stable at 2-8 °C, but should be kept at -20 °C for long term storage, preferably desiccated. Upon reconstitution, the preparation is stable for up to one week at 2-8 °C. For maximal stability, apportion the reconstituted preparation into working aliquots and store at -20 °C to -70 °C. Avoid repeated freeze/thaw cycles.
重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白
SDS-PAGE 重组人细胞周期蛋白依赖性激酶抑制剂2A,同种型1-TAT蛋白
Reference 1. Buda G, Maggini V, Galimberti S, et al. 2007. Leuk Res, 31: 569-70.
2. Komiya A, Suzuki H, Aida S, et al. 1995. Jpn J Cancer Res, 86: 622-5.
3. Jares P, Fernandez PL, Nadal A, et al. 1997. Oncogene, 15: 1445-53.
4. Mori T, Miura K, Aoki T, et al. 1994. Cancer Res, 54: 3396-7.
Background Cyclin-dependent kinase inhibitors (CDKIs) are proteins that bind to and inhibit the activity of CDKs. Two major classes of CDK inhibitors have been identified. The p16 family (p15, p16, p18 and p19) binds to and inhibits the activities of CDK4 and CDK6. The p21 family (p21, p27, p28 and p57) can bind to broad range of CDK-cyclin complexes and inhibit their activities. CDKIs are capable of suppressing growth, and several lines of evidence strongly suggest that at least some CDKIs may be tumor suppressor proteins. p16-INK4A is the member of p16 family and is encoded by CDKN2A gene in humans. It has three isoforms, which are wildly expressed but not detected in brain or skeletal muscle, except that isoform 3 is pancreas-specific. Defects in p16INK4A are a cause of Li-Fraumeni syndrome (LFS) and melanoma-astrocytoma syndrome (MASTS). The TAT transduction peptide can help rHuP16-INK4a with acrossing all kind of biomembranes in vivo and has no effect on the super structure of the protein.

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