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Merck
CN

T6567

Sigma-Aldrich

胰蛋白酶 来源于猪胰腺

Proteomics Grade, BioReagent, Dimethylated

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别名:
Porcine Trypsin, Trypsin for Mass Spectropetry
EC 号:
MDL编号:
UNSPSC代码:
12352204
NACRES:
NA.56

生物来源

Porcine pancreas

质量水平

产品线

BioReagent

溶解性

1 mM HCl: soluble 1 mg/mL, clear, colorless

运输

wet ice

储存温度

2-8°C

相关类别

一般描述

胰蛋白酶是一种丝氨酸蛋白酶,通常在生物化学和生物学中用作重要的酶试剂。这种方法产生了适用于蛋白质组学研究的高度纯化的胰蛋白酶产物。蛋白质组学等级非常适合用于溶液和凝胶胰蛋白酶消化。胰蛋白酶是一种丝氨酸蛋白酶,存在于几种脊椎动物的消化系统中。

应用

猪胰脏胰蛋白酶被应用于以下应用中:
  • 凝胶内蛋白消化及MALDI-TOF质谱分析
  • 电喷雾电离质谱(ESI-MS)分析
  • L. 植物杆菌的表面蛋白质组分析
  • 凝胶过滤,超离心,旋转阴影电子显微镜
  • 质谱

生化/生理作用

由于胰蛋白酶具有高度特异性裂解能力,胰蛋白酶肽数量有限,因此胰蛋白酶通常用于蛋白质组学研究中的肽定位和蛋白质序列研究。它可特异性地水解精氨酸和赖氨酸残基羧基侧的肽键。该酶还具有酯酶和酰胺酶的活性。胰蛋白酶作为一种细胞培养工具。在工业上,它被用来水解致敏蛋白以生产低致敏牛奶。

相关产品

产品编号
说明
价格

象形图

Health hazardExclamation mark

警示用语:

Danger

危险分类

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 1

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

动植物源性产品

分析证书(COA)

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What can I use to solubilize this Product T6567, Trypsin from porcine pancreas?

    This product is soluble in 1mM HCL.

  6. What is the package size of Product T6567, Trypsin from porcine pancreas?

    Each vial content 20 ug of the product.

  7. Is Product T6567, Trypsin from porcine pancreas, TPCK treated?

    The product has been treated with TPCK to remove chymotryptic activity, further purified through affinity chromatography, and lyophilized, resulting in convenient use and highly specific cleavage. This information is on the product page under application.

  8. How can we get Trypsin sequence information for Product T6567, Trypsin from porcine pancreas?

    If you are looking for trypsin sequence information, you have to go to the NCBI Protein Data Bank.

  9. How can we digest protein using Product T6567, Trypsin from porcine pancreas?

    As per Sigma R and D the information is as follows: In order to efficiently digest a protein with trypsin, it must be denatured and the disulfide bonds modified by reduction and alkylation, or at least reduced. Many intact proteins are highly resistant to digestion with trypsin. If you do not want to reduce and alkylate, you can then just boil the protein with 5 mM DTT or 20 mM 2ME for 10 minutes, and then quickly cool on ice to denature the protein. This may result in a precipitate, but the trypsin will still digest the protein and it will clear within an hour or two. You can also dissolve the protein in 6 M guanidine-HCl or 8 M urea. Reduce and alkylate using the PROT-RA kit or other suitable method. Then they would have to dilute the solution to less than 2 M of either denaturant and then add the trypsin. This is the method that we use routinely in the lab.

  10. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Masayuki Shimoda et al.
Cell transplantation, 21(2-3), 465-471 (2012-07-17)
Porcine islets are considered to be a promising resource for xenotransplantation. However, it is difficult to isolate porcine islets because of the marked fragility and rapid dissociation. Endogenous trypsin is one of the main factors to damage islets during the
Daniela M Remus et al.
Journal of bacteriology, 195(3), 502-509 (2012-11-24)
Sortases are transpeptidases that couple surface proteins to the peptidoglycan of Gram-positive bacteria, and several sortase-dependent proteins (SDPs) have been demonstrated to be crucial for the interactions of pathogenic and nonpathogenic bacteria with their hosts. Here, we studied the role
Hui Zheng et al.
Molecules (Basel, Switzerland), 18(11), 13425-13433 (2013-11-02)
A novel chemoenzymatic one-pot multicomponent synthesis of thiazole derivatives was developed. A series of thiazole derivatives were synthesized with high yields up to 94% under mild enzyme-catalyzed conditions. The blank and control experiments reveal that trypsin from porcine pancreas (PPT)
Maciej Suski et al.
Biochimica et biophysica acta, 1834(12), 2463-2469 (2013-08-31)
Excessive action of angiotensin II on mitochondria has been shown to play an important role in mitochondrial dysfunction, a common feature of atherogenesis and kidney injury. Angiotensin-(1-7)/Mas receptor axis constitutes a countermeasure to the detrimental effects of angiotensin II on
Fredrick Van Goor et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(46), 18843-18848 (2011-10-07)
Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene that impair the function of CFTR, an epithelial chloride channel required for proper function of the lung, pancreas, and other organs. Most patients with CF

商品

化学处理的重组胰蛋白酶在蛋白质组学和蛋白质表征分析中的应用评测

Evaluation of Recombinant, Chemically Treated Trypsin in Proteomics and Protein Characterization Assays

Pretreatment with Mucinase StcE increases glycopeptide identification from mucin samples, enhancing sample preparation efficiency for glycopeptide analysis.

The field of proteomics is continually looking for new ways to investigate protein dynamics within complex biological samples. Recently, many researchers have begun to use RNA interference (RNAi) as a method of manipulating protein levels within their samples, but the ability to accurately determine these protein amounts remains a challenge. Fortunately, over the past decade, the field of proteomics has witnessed significant advances in the area of mass spectrometry. These advances, both in instrumentation and methodology, are providing researchers with sensitive assays for both identification and quantification of proteins within complex samples. This discussion will highlight some of these methodologies, namely the use of Multiple Reaction Monitoring (MRM) and Protein-AQUA.

实验方案

本方案适用于使用Nα-苯甲酰基-L-精氨酸乙酯(BAEE)作为底物测定胰蛋白酶活性。本方案是基于连续分光光度速率测定(A253,光程= 1cm)方案:

Continuous spectrophotometric rate determination method using BAEE substrate measures trypsin activity, essential for enzyme characterization.

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