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Merck
모든 사진(1)

주요 문서

T1143

Sigma-Aldrich

Trypsinogen from bovine pancreas

essentially salt-free, lyophilized powder, ≥10,000 BAEE units/mg protein (E1%/280, after activation to trypsin)

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크기 선택

250 MG
₩429,345
1 G
₩1,184,099

₩429,345


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보기 변경
250 MG
₩429,345
1 G
₩1,184,099

About This Item

CAS Number:
EC Number:
UNSPSC 코드:
12352202
NACRES:
NA.56

₩429,345


재고 있음세부사항


생물학적 소스

bovine pancreas

Quality Level

분석

85-100% (UV)

양식

essentially salt-free, lyophilized powder

특이 활성도

≥10,000 BAEE units/mg protein (E1%/280, after activation to trypsin)

분자량

23,981 Da by calculation

기술

mass spectrometry (MS): suitable

solubility

H2O: soluble 10 mg/mL

UniProt 수납 번호

저장 온도

−20°C

유전자 정보

bovine ... TRYP8(282603)

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일반 설명

Trypsinogen is a proenzyme (zymogen) that is activated to form trypsin. It is synthesized in the pancreas and activated by enterokinase once it reaches the lumen of the small intestine. Bovine trypsinogen is a single polypeptide chain of 229 amino acids that is cross linked by six disulfide bridges. Enterokinase cleaves a hexapeptide to from the NH2 terminus of trypsinogen at the Lys6 - Ile7 peptide bond and activates it. Trypsin, thus formed, autocatalytically activates more trypsinogen to trypsin. This native form of trypsin is called β-trypsin, which undergoes autolysis at Lys131 - Ser132 resulting in α-trypsin that is held together by disulfide bridges. Trypsin is a serine protease with His46 and Ser183 at the active site.[1][2][3] The pH optimum of trypsin is 7 - 9.[4]

애플리케이션

Trypsinogen from bovine pancreas is suitable for use in:
  • the secondary structure analysis of proteins in H2O solution using single-pass attenuated total reflection Fourier transform infrared (ATR-FT-IR) microscopy[5]
  • tuning and calibration of electrospray ionization quadrupole time-of-flight (ESI-Q-TOF) mass spectrometer[6]
  • the secondary structure analysis of proteins by infrared (IR) spectroscopy[7]
  • SDS-PAGE as a molecular weight standard (24kDa)[8]

생화학적/생리학적 작용

Phytic acid complexed with calcium has been shown to increase the secretion of trypsinogen unable to be cleaved for activation. It also reduced the stabilization effect of calcium on activated trypsin.[9] The active form of trypsinogen, referred to as trypsin, cleaves peptides on the C-terminal side of lysine and arginine amino acid residues. It also hydrolyzes ester and amide linkages of synthetic derivatives of amino acids such as, benzoyl L-arginine ethyl ester (BAEE), p-toluenesulfonyl-L-arginine methyl ester (TAME), etc.[4][10][11]

단위 정의

One BAEE unit is equal to a ΔA253 of 0.001 per min with BAEE as substrate at pH 7.6 at 25 °C and a reaction volume of 3.2 mL (1 cm light path).

픽토그램

Health hazard

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Faceshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Burdon R H, et al.
Laboratory Techniques in Biochemistry and Molecular Biology, 9, 73-104 (1989)
H Klement et al.
European journal of biochemistry, 265(3), 862-874 (1999-10-16)
The enzyme NADPH:protochlorophyllide oxidoreductase (POR) is the key enzyme for light-dependent chlorophyll biosynthesis. It accumulates in dark-grown plants as the ternary enzyme-substrate complex POR-protochlorophyllide a-NADPH. Here, we describe a simple procedure for purification of pigment-free POR from etioplasts of Avena
The effect of calcium and phytic acid on the activation of trypsinogen and stability of trypsin.
Caldwell, R.
Journal of Agricultural and Food Chemistry, 40, 43-46 (1992)
Thomas M Dillon et al.
Journal of chromatography. A, 1053(1-2), 299-305 (2004-11-17)
Analytical characterization of monoclonal antibodies has been hindered by the lack of appropriate chromatographic methods to be used in conjunction with high-resolution MS. Current methodologies for standard RP-HPLC are incompatible with antibodies due to irreproducibility, low recovery, short column lifetimes
Rapid analysis of single-cysteine variants of recombinant proteins.
T W Keough et al.
Methods in molecular biology (Clifton, N.J.), 61, 171-183 (1996-01-01)

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