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- 保存条件:
低温
- 库存:
现货
- 供应商:
上海善然生物科技有限公司
- CAS号:
Trypsin-EDTA solution
Components
Trypsin consists of a single chain polypeptide of 223 amino acid residues, produced by the removal of the N-terminal hexapeptide from trypsinogen which is cleaved at the Lys - lle peptide bond. The sequence of amino acids is cross-linked by 6 disulfide bridges. This is the native form of trypsin, beta-trypsin. BETA-trypsin can be autolyzed, cleaving at the Lys - Ser residue, to produce alpha-trypsin. Trypsin is a member of the serine protease family.
Biochem/physiol Actions
Trypsin cleaves peptides on the C-terminal side of lysine and arginine residues. The rate of hydrolysis of this reaction is slowed if an acidic residue is on either side of the cleavage site and hydrolysis is stopped if a proline residue is on the carboxyl side of the cleavage site. The optimal pH for trypsin activity is 7-9. Trypsin can also act to cleave ester and amide linkages of synthetic derivatives of amino acids. EDTA is added to trypsin solutions as a chelating agent that neutralizes calcium and magnesium ions that obscure the peptide bonds on which trypsin acts. Removing these ions increases the enzymatic activity.
Serine protease inhibitors, including DFP, TLCK, APMSF, AEBSEF, and aprotinin, amongst others, will inhibit Trypsin.
Caution
This product is stored frozen between -10 and -40°C. Repeated cycles of freezing and thawing should be avoided.
Preparation Note
This product does contain phenol red. Due to shipment on dry ice, there could be significant carbon dioxide buildup in the package. This CO2 may enter the solution and lower the pH slightly, giving an orange rather than pinkish color. The orange solution will still be suitable for use, or the pH can be adjusted with sodium hydroxide. Incubating cells with too high a trypsin concentration for a long period can damage cell membranes and kill the cells. Solubilizing trypsin or diluting it from a concentrated solution should be done with a buffered salt solution containing no Ca2+ or Mg2+.
Application
The typical use for this product is in removing adherent cells from a culture surface. The concentration of trypsin necessary to dislodge cells from their substrate is dependent primarily on the cell type and the age of the culture.
性质
Related Categories Analytical and Industrial Enzymes, Application Index, Cell Dissociation, Cell Dissociation (Cell Culture Tested), Cell Dissociation and Cell Lysis,
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Quality Level GMP
sterility sterile-filtered
product line BioReagent
concentration 0.25%
impurities Porcine parvovirus, none detected (9 CFR)
pH-range 7.0 - 7.6
suitability suitable for cell culture
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文献和实验问:请问哪位仁兄能告知一下EDTA-胰蛋白酶的配制。急用!多谢!答:1、胰酶是0.25%,这是质量体积比,就是说0.25g胰酶溶于100ml PBS,注意,尽量不要用水来溶,因为要保持渗透压。2、EDTA的工作液溶度是0.02%-0.1%,根据细胞消化的难易程度自己调整。EDTA并不是必须的,容易消化的细胞可不加。EDTA对细胞贴壁性有影响,因此使用时要甚重。如果影响贴壁,但消化时必须要用,那么在用完全培养基终止消化后,可离心弃上清,再加完全培养基培养,可去除EDTA。如果对贴壁没
蛋白沉淀出来。经硫酸铵分级盐析将胰蛋白酶原、胰凝乳蛋白酶原和弹性蛋白酶原沉淀。沉淀物经水溶解并调至pH8.0,用极少量的胰蛋白酶将胰蛋白酶原激活,同时溶液中的胰凝乳蛋白酶原和弹性蛋白酶原也被激活,三种酶原相互作用过程如下: 也可采用从胰脏中提取出胰蛋白酶原,利用合适的提取溶液的pH值促使胰蛋白酶原部分自溶,并通过溶液中Ca2+的环境,使胰蛋白酶原被开始自溶的少量具有活性的胰蛋白酶所激活,转变为具有活性的胰蛋白酶(胰凝乳蛋白酶原及弹性蛋白酶原亦同时被胰蛋白酶激活成有活性的酶
,一般多用的浓度是0.02% 可以用不含钙镁的平衡盐溶液溶解,水也可以然后灭菌分装,你可以用稍微量大一点的胰酶而不用EDTA,要是直接都用EDTA你的细胞要是都能消化下来,也是可以的,但是注意消化以后用HANKS 来清洗残留的EDTA。 wangruimishu 可能是我的细胞比较容易存活的原因吧,我只用EDTA消化,细胞长的还可以,只是感觉消化的慢 本文由丁香园论坛提供,想了解更多有用的、有意思的前沿资讯以及酷炫的实验方法的你,都可以成为师兄
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