M-MLV Reverse Transcriptase (200 U/μL)
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M-MLV Reverse Transcriptase (200 U/μL)
Invitrogen™

M-MLV Reverse Transcriptase (200 U/μL)

M-MLV (Moloney Murine Leukemia Virus) Reverse Transcriptase (RT)은 single-stranded RNA, DNA 또는 RNA:DNA hybrid에서 보상적 DNA strand를 합성하는 재조합 DNA자세히 알아보기
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카탈로그 번호반응 수
28025013200 Reactions
280250211,000 Reactions
카탈로그 번호 28025013
제품 가격(KRW)
475,000
온라인 행사
Ends: 31-Dec-2025
527,000
할인액 52,000 (10%)
Each
카트에 추가하기
반응 수:
200 Reactions
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
475,000
온라인 행사
Ends: 31-Dec-2025
527,000
할인액 52,000 (10%)
Each
카트에 추가하기
M-MLV (Moloney Murine Leukemia Virus) Reverse Transcriptase (RT)은 single-stranded RNA, DNA 또는 RNA:DNA hybrid에서 보상적 DNA strand를 합성하는 재조합 DNA polymerase입니다. AMV RT과 비교해 M-MLV RT은 DNA endonuclease 활성이 없고 RNase H 활성이 낮습니다.

열안정성 – 37°C에서 최적 활성
cDNA 크기 – MMLV은 최대 7kb의 first-strand cDNA 합성에 사용할 수 있습니다.
적용 – first-strand cDNA 합성(1), primer extension (2), sequencing dsDNA (3), cDNA libraries, RT-PCR (4)

원천: plasmid에서 M-MLV의 pol gene을 발현하는 E. coli에서 정제함 (5).

성능 및 품질 시험: SDS-PAGE 순도, endodeoxyribonuclease, exodeoxyribonuclease, ribonuclease assays, cDNA 산물 길이 및 수율.

단위 정의: M-MLV RT 한 단위는 template• primer로 poly(A)• oligo(dT)12-18를 사용해 37°C 에서 10분 내에 deoxyribonucleotide 1 nmole을 acid-precipitable 물질에 통합시키는데 필요한 효소 양입니다 (6).

단위 반응 조건: 50 mM Tris-HCl (pH 8.3), 40 mM KCl, 6 mM MgCl2, 1 mM DTT, 0.5 mM [3H]dTTP, 0.1 mM poly(A), 0.1 mM oligo(dT)12-18, 0.1 mg/ml BSA, enzyme 50 μl - 37°C에서 10분 (6).

이 제품은 연구용으로만 사용가능합니다. 치료 또는 진단 목적으로 동물이나 인간에 사용할 수 없습니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
최종 제품 유형First-Strand cDNA
형식Stand-alone Enzyme
반응 수200 Reactions
최적 반응 온도37°C
수량40,000 units
반응 형식Separate components
시약 유형Reverse Transcription
역전사 효소M-MLV
리보뉴클레아제 H 활성Yes
배송 조건Wet Ice
크기(최종 제품)Up to 7 kb
시작 물질RNA
기술Reverse Transcription
농도200 U/μL
반응 속도50 min.
Unit SizeEach
구성 및 보관

• M-mLV RT, 200 μL (200 U/μL)
• 5X First Strand Buffer, 1 mL
• DTT, 500 μL (100 mM)

Store at –20°C.

자주 묻는 질문(FAQ)

How much of the first-strand cDNA reaction should I load for PCR?

While the volume is dependent on the starting amount of RNA used for the first-strand synthesis and the abundance of the target gene, we'd recommend starting with 10% of the first-strand reaction for your PCR reaction.

How can reverse transcriptases be inactivated?

The enzymes can be inactivated by adding a chelating agent such as EDTA. Alternatively, with the exception of ThermoScript RT and Thermo-X RT, the enzymes can be heat inactivated at 70 degrees C for 10 min.

ThermoScript RT should be heated to 85 degrees C for 5 min for complete inactivation.

For Thermo-X RT, if using an oligo(dT) primer, add EDTA to the reaction at a final concentration of 5 mM. Inactivate the reaction by heating at 90 degrees C for 5 min.

What is the highest temperature that MMLV, SuperScript II, SuperScript III, or SuperScript IV RTs can be used?

The optimal temperature for for MMLV is 42 degrees C. The optimal temperature for SuperScript II RT is 42 degrees C, and can be used up to 50 degrees C. The optimal temperature for SuperScript III RT is 50 degrees C, and can be used up to 55 degrees C. For some qRT-PCR reactions where gene-specific primers are used, you can do the RT reaction at 60 degrees C. The optimal temperature for SuperScript IV RT is 50 degrees C, but can be used up to 65 degrees C.

Can I use a DNA-RNA hybrid as a template for M-MLV Reverse Transcriptase (Cat. No. 28025013, 28025021)? Can other reverse transcriptases, such as SuperScript reverse transcriptase, be used in the same way?

Yes, you can use a DNA-RNA hybrid as a template for M-MLV Reverse Transcriptase.

We have not tested this for SuperScript reverse transcriptases, so we cannot guarantee it would also work with those products.

This article can be used as a reference for additional information.

Find additional tips, troubleshooting help, and resources within our Reverse Transcription and RACE Support Center.

Can I use elevated temperatures for reverse transcription with Moloney Murine Leukemia Virus (M-MLV) reverse transcriptase?

Moloney Murine Leukemia Virus (M-MLV) Reverse Transcriptase is not well-suited for elevated temperatures. Typically, M-MLV RT operates optimally at temperatures around 37 degrees C to 42 degrees C.

To perform reverse transcription at elevated temperatures (e.g., 50 degrees C or higher), consider using thermostable reverse transcriptases such as SuperScript IV or Maxima H Minus, which are engineered to perform efficiently at higher temperatures.

인용 및 참조 문헌 (4)

인용 및 참조 문헌
Abstract
Raloxifene Upregulated Mesangial Cell MMP-2 Activity via ER-ß Through Transcriptional Regulation.
Authors:Fang M, Wu XC, Huang W,
Journal:Cell Biochem Biophys
PubMed ID:23471663
'Raloxifene, a second-generation selective estrogen receptor modulator, exerts estrogen-like effects in specific tissues. In this present study, we examined the effect of raloxifene on mesangial cell matrix metalloproteinase-2 (MMP-2) activity in streptozotocin-induced diabetic mice. Raloxifene increased the MMP-2 level in a dose-dependent and receptor-mediated manner. An antibody against estrogen receptor-ß ... More
Single cell rt-PCR identification of odorant receptors expressed by olfactory neurons.
Authors:Malnic B,
Journal:Methods Mol Biol
PubMed ID:23585038
'Mammals have between 400 and 1,300 functional odorant receptor (OR) genes in their genomes. Each olfactory sensory neuron in the nose expresses only one single type of OR out of this vast repertoire. The OR expressed by an olfactory sensory neuron determines its functional activity and wiring to the olfactory ... More
Fast-mode duplex qPCR for BCR-ABL1 molecular monitoring: innovation, automation, and harmonization.
Authors:Gerrard G, Mudge K, Foskett P, Stevens D, Alikian M, White HE, Cross NC, Apperley J, Foroni L,
Journal:Am J Hematol
PubMed ID:22566190
Reverse transcription quantitative polymerase chain reaction (RTqPCR)is currently the most sensitive tool available for the routine monitoring of disease level in patients undergoing treatment for BCRABL1 associated malignancies. Considerable effort has been invested at both the local and international levels to standardise the methodology and reporting criteria used to assess ... More
Transforming growth factor-ß is required for vasculogenic mimicry formation in glioma cell line U251MG.
Authors:Ling G, Wang S, Song Z, Sun X, Liu Y, Jiang X, Cai Y, Du M, Ke Y,
Journal:Cancer Biol Ther
PubMed ID:22104964
Both vasculogenic mimicry (VM) and transforming growth factor-ß (TGFß) are positively correlated with malignancy in glioma. Accordingly, we supposed that TGFß might be related with VM, and aimed to detect whether TGFß could influence VM formation in two glioma cell lines U251MG and SHG44, which were different in malignancy. We ... More