Bsa I GMP-grade (20 U/μL)-酶-试剂-生物在线
翌圣生物科技(上海)股份有限公司
Bsa I GMP-grade (20 U/μL)

Bsa I GMP-grade (20 U/μL)

商家询价

产品名称: Bsa I GMP-grade (20 U/μL)

英文名称: Bsa I GMP-grade (20 U/μL)

产品编号: 10661ES03

产品价格: 1035.00

产品产地: yeasen

品牌商标: yeasen

更新时间: 2024-12-10T13:22:33

使用范围: null

规格 价格
1 KU 1035.0
10 KU 7245.0
100 KU 36225.0
翌圣生物科技(上海)股份有限公司
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Product description

 

This product is a type IIS restriction endonuclease derived from the recombinant protein encoded by the BsaI gene in Bacillus sphaericus expressed by E.coli. Its recognition sequence is 5'-GGTCTCN1/N5-3'. Use to digest plasmids to prepare poly(A/T/G/C)-terminated linearized DNA fragments to obtain specific cohesive ends.

This product is produced in accordance with GMP process requirements and provided in a liquid form.

 

Specifications

 

Expression Host

Recombinant E. coli with BasI gene

Reaction Temperature

37℃

Storage Buffer

10 mM Tris-HCl, 0.2 M NaCl, 0.1 mM EDTA, 1mM DTT, 50% Glycerol

Unit Definition

1 unit: The amount of enzyme required to digest 1 μg of substrate DNA within 1 h at 37℃ in a 50 μL system.

Application

1.Digest the plasmid to prepare a linearized DNA fragment at the end of Poly (A/T/C/G);

2.Digestion of DNA to obtain specific sticky ends;

3.Linearize plasmid template before in-vitro transcription.

 

Components

 

Components No.

 

Name

10661ES03

(1 KU)

10661ES10

(10 KU)

10661ES60

(100 KU)

10661

BsaI GMP-grade (20 U/μL)

50 μL

500 μL

5 mL

 

Storage

 

This product should be stored at -25 ~ -15℃ for two years.

 

Instructions

 

Experimental methods

50 μL reaction system

This step is suitable for linearization of 1 μg DNA (≥100 nt) and can be scaled up according to experimental needs.

1. Add the following components in sequence:

Components

Volume

Plasmid DNA

1-2 μg

10×Digestion Buffer 4

5.0 μL

BsaI (20 U/μL)

1.0 μL

RNase-free ddH2O

Up to 50 μL

【Note】10× Digestion Buffer 4(Cat#10668ES): 500 mM Potassium Acetate,200 mM Tris-acetate,100 mM Magnesium Acetate,1 mg/ml OsrHSA, pH7.9@25℃

2. Incubate at 37°C 1 h;

3. DNA linearization is complete, and subsequent experiments can be performed.

 

Notes

 

1. Heat inactivation condition: incubate at 80°C for 20min.

2. Please operate with lab coats and disposable gloves,for your safety.

 

 

Ver.EN20230725