콘텐츠로 건너뛰기
Merck
모든 사진(1)

주요 문서

SMAI-RO

Roche

Sma I

from Serratia marcescens Sb

로그인조직 및 계약 가격 보기


About This Item

UNSPSC 코드:
12352204

생물학적 소스

Serratia marcescens

Quality Level

양식

solution

특이 활성도

10000 U/mL

포장

pkg of 1,000 U (10220566001 [10 U/μl])
pkg of 5,000 U (10656348001 [10 U/μl])
pkg of 5,000 U (11047639001 [40 U/μl])

제조업체/상표

Roche

농도

<0.1 % (w/w)

파라미터

25 °C optimum reaction temp.

기술

electrophoresis: suitable

색상

colorless

pH

7.0 (39 °F)

solubility

water: miscible

적합성

suitable for molecular biology

응용 분야

life science and biopharma

외래 활성

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

배송 상태

dry ice

저장 온도

−20°C

관련 카테고리

일반 설명

Sma I recognizes the sequence *C°C*C↓GGG and generates fragments with blunt ends.

특이성

Recognition sites: *C °C*CGGG
*C °C*CGGG
Restriction site: *C °C*C↓GGG
*C °C*C↓GGG
Heat inactivation: Sma I can be heat inactivated by incubation at 65 °C for 15 minutes (up to 100 U/μg DNA).

애플리케이션

Sma I has been used in macrorestriction analysis. It has also been used in the restriction enzyme mixture during restriction digestion, amid rapid pulsed-field gel electrophoresis (PFGE).

품질

Absence of nonspecific endonuclease activities
1μg λDNA is incubated for 16 hours in 50μl SuRE/Cut Buffer A with an excess of Sma 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 5μg [3H] labeled calf thymus DNA are incubated with 3μl Sma I for 4 hours at +37°C in a total volume of 100μl 50mM Tris-HCl, 10mM MgCl2, 1mM Dithioerythritol, pH approximately 7.5. Under these conditions, no release of radioactivity is detectable, as stated in the certificate of analysis.

DNA 프로파일

Number of cleavage sites on different DNAs
  • λ: 3
  • φX174: 0
  • Ad2: 12
  • M13mp7: 0
  • pBR322: 0
  • pBR328: 0
  • pUC18: 1
  • SV40: 0

단위 정의

One unit is the enzyme activity that completely cleaves 1 μg λDNA in one hour at +25 °C in a total volume of 25 μl (1x) SuRE/Cut buffer A.

저장 및 안정성

Do not store below −25°C

분석 메모

Compatible ends
Sma I generates ends that are compatible with any blunt end.

Isoschizomers

The enzyme is an isoschizomer to Cfr9 I, PspA I, Xma I, and XmaC I.

Methylation sensitivity
Sma I is not inhibited by 5-methylcytosine at the middle of the three C residues (°) in the recognition sequence. However, the activity is inhibited by 5-methylcytosine at the other Cs (*) or 4-methylcytosine in any position within the recognition sequence (*C°C*C↓GGG).

Incubation temperature
+25°C

PFGE tested
Sma 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 10 U of enzyme/μg DNA and 4 hour incubation time.

Ligation and recutting assay

Sma I fragments obtained by complete digestion of 1μg λDNA are ligated with 1U T4 DNA Ligase in a volume of 10μl by incubation for 16 hours at +25°C in 66mM Tris-HCl, 5mM MgCl2, 5mM Dithioerythritol, and 1mM ATP, pH 7.5 (at +20°C) resulting in >80% recovery of 1μg λDNA fragments.
Subsequent re-cutting with Sma I yields >80% of the typical pattern of λDNA × Sma I fragments.
SuRE/Cut Buffer System
The buffer in bold is recommended for optimal activity
  • A: 100%
  • B: 0-10%
  • H: 0-10%
  • L: 0-10%
  • M: 0-10%

Activity in PCR buffer: 100%

Relative activity in PCR mix (Taq DNA Polymerase buffer) is 100%. The PCR mix contained λDNA, primers, 10 mM Tris-HCl (pH 8.3, 20 °C), 50 mM KCl, 1.5 mM MgCl2, 200 μM dNTPs, 2.5 U Taq DNA polymerase. The mix was subjected to 25 amplification cycles.Activity in reaction buffer of Pwo SuperYield DNA Polymerase PCR Mix is 100%. If supplemented with GC-RICH Solution, activity remains at 100%. Pwo SuperYield DNA Polymerase PCR Mix is not available in U.S.

기타 정보

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

키트 구성품 전용

제품 번호
설명

  • Enzyme Solution

  • SuRE/Cut Buffer A 10x concentrated

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point (°F)

does not flash

Flash Point (°C)

does not flash


가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number

적합한 버전을 찾을 수 없으신가요?

특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Corinna Kehrenberg et al.
Antimicrobial agents and chemotherapy, 51(2), 483-487 (2006-12-06)
During a study of florfenicol-resistant porcine staphylococci from Denmark, the genes cfr and fexA were detected in the chromosomal DNA or on plasmids of Staphylococcus hyicus, Staphylococcus warneri, and Staphylococcus simulans. A novel variant of the phenicol resistance transposon Tn558
E M Ribot et al.
Journal of clinical microbiology, 39(5), 1889-1894 (2001-04-28)
We developed a rapid pulsed-field gel electrophoresis (PFGE) protocol for subtyping Campylobacter isolates based on the standardized protocols used by PulseNet laboratories for the subtyping of other food-borne bacterial pathogens. Various combinations of buffers, reagents, reaction conditions (e.g., cell suspension

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.

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

고객지원팀으로 연락바랍니다.