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10661ESBsa I限制性內(nèi)切酶GMP-grade
參考價1035-36225
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  • 10661ES 型號
  • Yeasen/翌圣生物 品牌
  • 生產(chǎn)商 廠商性質(zhì)
  • 上海市 所在地

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1 KU1035元99 件 可售
10 KU7245元99 件 可售
100 KU36225元99 件 可售

訪問次數(shù):464更新時間:2025-01-23 13:53:21

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初級會員·13年
聯(lián)人:
曹女士
話:
400-6111-883
機:
后:
4006-111-883
真:
86-21-34615995
址:
上海市浦東新區(qū)天雄路166弄1號3樓
網(wǎng)址:
www.yeasen.com

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產(chǎn)品簡介
供貨周期 現(xiàn)貨 貨號 10661ES
應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,生物產(chǎn)業(yè)
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
產(chǎn)品介紹

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 Bas I gene

Reaction Temperature

37℃

Storage Buffer

10mM Tris-HCl, 0.2M NaCl, 0.1mM EDTA, 1mM DTT, 50% Glycerol, 0.2mg/ml OsrHSA pH 7.4±0.2 (25℃)

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

Bsa I 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.

1Add the following components in sequence:

 

Components

Volume

Plasmid DNA

1-2 μg

10×Digestion Buffer 4

5.0 μL

Bsa I (20 U/μL)

1.0 μL

RNase-free ddH2O

Up to 50 μL

Note10× Digestion Buffer 4(Cat#10668ES): 500 mM Potassium Acetate,200 mM Tris-acetate,100 mM Magnesium Acetate,1 mg/ml OsrHSA, pH7.9@25℃

2Incubate at 37°C 1 h;

3DNA 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.

 

 




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