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T4799

Trypsin from porcine pancreas

lyophilized powder, BioReagent, suitable for cell culture, 1,000-2,000 BAEE units/mg solid

Trypsin from porcine pancreas

Synonyma:

Cocoonase, Tryptar, Tryptase

Přihlásit pro zobrazení organizačních a smluvních cen.

Vybrat velikost

Změnit zobrazení
Velikost baleníSkladová položkaDostupnostCena
5 g
Obraťte se na zákaznický servis a vyžádejte si informaci o dostupnosti.
854,00 Kč
10 g
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1 600,00 Kč
25 g
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2 840,00 Kč
10 x 5 g
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6 660,00 Kč
100 g
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8 290,00 Kč
500 g
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48 700,00 Kč

O této položce

Číslo CAS:
UNSPSC Code:
12352204
NACRES:
NA.75
EC Number:
232-650-8
MDL number:
Číslo EC:
Specific activity:
1,000-2,000 BAEE units/mg solid
Biological source:
Porcine pancreas
Concentration:
25 mg/mL

854,00 Kč


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biological source

Porcine pancreas

Quality Level

product line

BioReagent

form

lyophilized powder

specific activity

1,000-2,000 BAEE units/mg solid

mol wt

23.8 kDa

concentration

25 mg/mL

technique(s)

cell culture | mammalian: suitable, single cell analysis: suitable

pH

7.6

shipped in

ambient

storage temp.

−20°C

General description

Trypsin is applicable for tissue disaggregation, due to its effective action and tolerance towards different cell type and serum-induced neutralization.

Application

For trypsin digestion of peptides, use a ratio of about 1:100 to 1:20 for trypsin:peptide. 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. Trypsins have also been used for the re-suspension of cells during cell culture, in proteomics research for digestion of proteins and in various in-gel digestionsns†. Additional applications include assessing crystallization by membrane-based techniques and in a study to determine that protein folding rates and yields can be limited by the presence of kinetic traps.
Trypsin from porcine pancreas has been used to digest chicken bones. It has also been used in the isolation of luteal endothelial cells.

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.

Preparation Note

This product is a lyophilized powder soluble in Hank′s Balanced Salt Solution at 25 mg/mL.
For applications that require EDTA, solubilizing trypsin should be done with a buffered salt solution contaiing no Ca2+ or Mg2+.

Other Notes

One BAEE unit will produce a ΔA253 of 0.001 per min at pH 7.6 at 25° C using BAEE as substrate. One BTEE unit = 320 ATEE units. Reaction volume = 3.2 mL (1 cm light path).
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.

Disclaimer

Solutions in 1 mM HCl are stable for 1 year in aliquots and stored at -20°C. The presence of Ca2+ will also diminish the self-autolysis of trypsin and maintain its stability in solution. Trypsin will also retain most of its activity in 2.0 M urea, 2.0 M guanidine HCl, or 0.1% (w/v) SDS.

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Tato položka
T8802T6424T7168
technique(s)

cell culture | mammalian: suitable, single cell analysis: suitable

technique(s)

-

technique(s)

-

technique(s)

-

biological source

Porcine pancreas

biological source

bovine pancreas

biological source

human pancreas

biological source

Porcine pancreas

specific activity

1,000-2,000 BAEE units/mg solid

specific activity

≥10,000 BAEE units/mg protein

specific activity

-

specific activity

90-110% (compared to standard)

concentration

25 mg/mL

concentration

-

concentration

-

concentration

-

form

lyophilized powder

form

essentially salt-free, lyophilized powder

form

salt-free, lyophilized powder

form

tablet

pH

7.6

pH

-

pH

-

pH

-


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pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Skladovací třída

11 - Combustible Solids

wgk

WGK 1

ppe

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



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Protokoly

Kontinuální spektrofotometrická metoda stanovení rychlosti pomocí substrátu BAEE měří aktivitu trypsinu, která je nezbytná pro charakterizaci enzymu.

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


Prostaglandin F2alpha regulates the nitric oxide generating system in bovine luteal endothelial cells
Lee SH, et al.
Journal of Reproduction and Development, 55(4), 418-424 (2009)
The development of angiotensin I-converting enzyme inhibitor derived from chicken bone protein
Animal Science Journal = Nihon Chikusan Gakkaiho, 79(1), 122-128 (2008)
Effects of tumor necrosis factor alpha and Interferon gamma on the viability and mRNA expression of TNF receptor type I in endothelial cells from the bovine corpus luteum
Hojo T, et al.
Journal of Reproduction and Development, 56(5), 515-519 (2010)



Globální číslo obchodní položky

Skladová položkaGTIN
T4799-25G04061835569601
T4799-10G04061835569595
T4799-500G04061835569618
T4799-10X5G04061837346743
T4799-5G04061835569625
T4799-100G04061835569588

Questions

  1. Is this pure trypsin? there any excipient in the product?

    1 answer
    1. Quantitave purity testing is not performed on this product. While there may be residual salts and trace components present following the purification process, no specific excipients have been added. This material has not been TCPK-treated.

      Helpful?

Reviews

Active Filters

  1. East Lansing Michigan
    • Reviews 4
    • Votes 5
    5 out of 5 stars.

    MSU lab Manager

    I like to buy Trypsin from porcine pancreas from Sigma because is a product with high-quality control.

    Helpful?