EKMax™ Enterokinase
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Invitrogen™

EKMax™ Enterokinase

EKMax™는 bovine enterokinase의 촉매소단위 재조합품입니다(1). EKMax™는 Asp-Asp-Asp-Asp-Lys 서열을 인식하고 lysine 잔기 다음 펩티드 결합을 절단합니다. 이 효소는 이런 펩티드 서열을자세히 알아보기
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카탈로그 번호수량
E180021000 Units
E18001250 Units
카탈로그 번호 E18002
제품 가격(KRW)
3,916,000
Online offer
Ends: 31-Dec-2025
4,607,000
할인액 691,000 (15%)
Each
카트에 추가하기
수량:
1000 Units
제품 가격(KRW)
3,916,000
Online offer
Ends: 31-Dec-2025
4,607,000
할인액 691,000 (15%)
Each
카트에 추가하기
EKMax™는 bovine enterokinase의 촉매소단위 재조합품입니다(1). EKMax™는 Asp-Asp-Asp-Asp-Lys 서열을 인식하고 lysine 잔기 다음 펩티드 결합을 절단합니다. 이 효소는 이런 펩티드 서열을 가진 fusion protein을 절단하는 데도 사용할 수 있습니다(그림 1).

어플리케이션: 재조합 단백질에서 fusion tag 제거.

단위 정의: EKMax™ 한 단위는 37°C에서 16시간동안 thioredoxin-CAT fusion protein 20 μg을 90% digest하는데 필요한 효소 양입니다. EKMax™ 한 단위는 ∼190 trypsinogen 활성단위에 해당합니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
제품 유형Enterokinase
수량1000 Units
Cattle/Bovine
제품라인EKMax
Unit SizeEach
구성 및 보관
EKMax™ Enterokinase is provided with 10X buffer. Store at -20°C. Guaranteed stable for 6 months when stored properly.

자주 묻는 질문(FAQ)

What is the molecular weight of the EKMax enterokinase enzyme?

EKMax enterokinase is a clone of the catalytic subunit of enterokinase expressed in the yeast Pichia pastoris. The calculated molecular weight of the protein is 26.3 kDa, but it contains three sites for asparagine-linked glycosylation. The apparent molecular weight of 43 kDa is consistent with previous observations (LaVallie et al., 1993) and is assumed to be because of N-linked glycosylation.
Reference: LaVallie, E.R., Rehemtulla, A., Racie, L.A.,Diblasio, E.A., Ferenz, C., Grant, K.L. Light, A., and McCoy, J.M. (1993). Cloning and functional expression of a cDNA encoding the catalytic subunit of bovine enterokinase. J.Biol.Chem. 268, 23311-23317.

Will DTT, Triton X-100 detergent, Tween 20 detergent, Thesit, calcium chloride, sodium chloride, or SDS affect the efficiency of Enterokinase (EKMax) enzyme cleavage?

Enterokinase is active in buffers containing up to 1 mM DTT, 0.1% Triton X-100 detergent, 0.1% Tween 20 detergent, and 0.1% Thesit. It is recommended to have 10mM Tris pH 8.0 and 10 mM calcium chloride in the buffer. Enterokinase is inhibited by sodium chloride and SDS.

Should Enterokinase be resuspended in a buffer containing 50% glycerol to protect the protein from freeze/thaw cycles?

Freeze thaw has a minimal effect on the activity of Enterokinase. The addition of glycerol is not necessary but can make handling of the enzyme easier.

How specific is cleavage by EKMax Enterokinase? Are there any alternate cleavage sites for the enzyme?

Enterokinase cleaves after the sequence (Asp)4-Lys.

It has been proposed that the active center of enterokinase possesses a distinctive cationic subsite that binds -(Asp)4. Enterokinase is highly specific and tolerates very few changes to its recognition site. If the ionic charge of the recognition site is preserved, enterokinase will recognize the site, but the rate of hydrolysis of the peptide bond will be reduced (Light and Janska, 1989). The four aspartyl residues act as a signal for enterokinase cleavage. It has been reported that with only three aspartyl residues the rate of hydrolysis is reduced. Two aspartyl residues preceding the lysyl residue are the minimum number of acidic residues needed to maintain specificity (Maroux et al., 1971). Non-specific cleavage by enterokinase may occur in the cases described above, but this is usually alleviated by reducing the amount of enzyme used.

What products do you offer for enzymatic cleavage of fusion tags from recombinant proteins?

We offer the following products:

-AcTEV Protease (Cat. Nos. 12575015, 12575023)
-EKMax Enterokinase (Cat. Nos. E18001, E18002)
-SUMO Protease (Cat. No. 12588018)


Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

인용 및 참조 문헌 (1)

인용 및 참조 문헌
Abstract
Interaction of the Conserved Region 4.2 of sigma E with the RseA Anti-sigma Factor.
Authors: Tam Christina; Collinet Bruno; Lau Gary; Raina Satish; Missiakas Dominique;
Journal:J Biol Chem
PubMed ID:12016219
Evarsigma(E) RNA polymerase transcribes a regulon of folding factors for the bacterial envelope and is induced by physical and chemical stresses. The RseA anti-sigma factor inhibits the activity of Evarsigma(E) RNA polymerase. It is shown here that the N-terminal portion of varsigma(E), residues 1-153, binds core RNA polymerase. RseA interacts ... More