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BLNI-RO

Roche

Bln I (Avr II)

from Brevibacterium linens

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About This Item

UNSPSC 코드:
12352204

생물학적 소스

bacterial (Brevibacterium linens)

Quality Level

형태

solution

특이 활성도

10000 U/mL

포장

pkg of 1,000 U (11558170001 [10 U/μl])
pkg of 200 U (11558161001 [10 U/μl])

제조업체/상표

Roche

파라미터

37 °C optimum reaction temp.

색상

colorless

pH

8.1 (39 °F)

solubility

water: miscible

적합성

suitable for molecular biology

응용 분야

life science and biopharma
sample preparation

외래 활성

Endonucleases, none detected (up to 20 U with MWM II-DNA)
Endonucleases, none detected (up to 20U with pBR 322-DNA)

배송 상태

dry ice

저장 온도

−20°C

일반 설명

Bln I recognizes the sequence C↓CTAGG and generates fragments with 5′-cohesive termini.

Compatible ends
Bln I ends are compatible with ends generated by Nhe I, Spe I and Xba I.

Isoschizomers
Bln I is an isoschizomer of Avr II.
Note: The complete 13 site Avr II restriction map of the E.coli genome has been reported.

Methylation sensitivity
The enzyme is not known to be affected by methylation.

특이성

Recognition sites: CCTAGG
CCTAGG
Restriction site: C↓CTAGG
C↓CTAGG
Heat inactivation: No inactivation of Bln I after incubation at 65 °C for 15 minutes.

품질

Absence of nonspecific endonuclease activities
1 μg λDNA is incubated for 16 hours in 50 μl SuRE/Cut Buffer H with an excess of Bln I. The number of enzyme units which do not change the enzyme-specific pattern is stated in the certificate of analysis.

Absence of exonuclease activity
Approximately 5 μg [3H] labeled calf thymus DNA are incubated with 3 μl Bln I for 4 hours at +37°C in a total volume of 100 μl 50 mM Tris-HCl, 10 mM MgCl2, 1 mM Dithioerythritol, pH approximately 7.5. Under these conditions, no release of radioactivity is detectable, as stated in the certificate of analysis.

Typical ligation and recutting assay
Bln I fragments obtained by complete digestion of 1 μg λ × EcoR I DNA ligated for 16 hours at +4°C with 1 U T4 DNA Ligase in 10 μl buffer that contains 66 mM Tris-HCl, 5 mM MgCl2, 5 mM Dithiothreitol, 1 mM ATP, pH 7.5 (at +20°C). The percentages of product that can be ligated and subsequently recut with Bln I and EcoR I (yielding the typical pattern of λ × EcoR I × Bln I fragments) are stated under "Lig" and "Rec" in the certificate of analysis.

DNA 프로파일

Number of cleavage sites on different DNAs
  • λ: 2
  • φX174: 0
  • Ad2: 2
  • M13mp7: 0
  • M13mp18:0
  • pBR322: 0
  • pBR328: 0
  • pUC18: 0
  • SV40: 2

단위 정의

One unit is the enzyme activity that completely cleaves 1 μg λ x EcoR I DNA fragments in one hour at +37 °C in a total volume of 25 μl (1x) SuRE/Cut Buffer H.

저장 및 안정성

Do not store below −25°C.

분석 메모

PFGE tested
Bln I has been tested in Pulsed-Field Gel Electrophoresis (on bacterial chromosomes). For cleavage of genomic DNA (E.coli C 600) embedded in agarose for PFGE analysis, we recommend using 10 U of enzyme/μg DNA and 4 hour incubation.
SuRE/Cut Buffer System
The buffer in bold is recommended for optimal activity
  • A: 25-50%
  • B: 50-75%
  • H: 100%
  • L: 0-10%
  • M: 25-50%

Activity in PCR buffer: Not tested

기타 정보

For life science research only. Not for use in diagnostic procedures.

키트 구성품 전용

제품 번호
설명

  • Enzyme Solution

  • SuRE/Cut Buffer H 10x concentrated

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point (°F)

does not flash

Flash Point (°C)

does not flash


시험 성적서(COA)

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문서

The term “Restriction enzyme” originated from the studies of Enterobacteria phage λ (lambda phage) in the laboratories of Werner Arber and Matthew Meselson.

관련 콘텐츠

Restriction endonucleases popularly referred to as restriction enzymes, are ubiquitously present in prokaryotes. The function of restriction endonucleases is mainly protection against foreign genetic material especially against bacteriophage DNA.

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