M-MLV Reverse Transkriptase (200 U/μl)
Invitrogen™

M-MLV Reverse Transkriptase (200 U/μl)

M-MLV Reverse Transkriptase ist eine rekombinante DNA-Polymerase, die aus einsträngiger RNA, DNA oder einem RNA:DNA-Hybrid einen DNA-Komplementärstrang synthetisiert. Im VergleichWeitere Informationen
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KatalognummerAnzahl Reaktionen
28025013200 Reaktionen
280250211.000 Reaktionen
Katalognummer 28025013
Preis (EUR)
486,00
Each
Anzahl Reaktionen:
200 Reaktionen
Großbestellung oder individuelle Größe anfordern
Preis (EUR)
486,00
Each
M-MLV Reverse Transkriptase ist eine rekombinante DNA-Polymerase, die aus einsträngiger RNA, DNA oder einem RNA:DNA-Hybrid einen DNA-Komplementärstrang synthetisiert. Im Vergleich zu AMV RT besitzt Moloney Murine Leukemia Virus Reverse Transkriptase (M-MLV RT) nur eine geringfügige Aktivität von DNA-Endonuklease und RNase H. Merkmale dieses Enzyms:

Thermostabilität – optimale Aktivität bei 37 °C
cDNA-Größe – M-MLV kann zum Synthetisieren von Erststrang-cDNA bis zu 7 kb eingesetzt werden
Anwendungen – Synthese von Erststrang-cDNA, Primer-Verlängerung, Sequenzierung von dsDNA, cDNA-Bibliotheken und RT-PCR

Quelle
Aufgereinigt aus E. coli, das das pol-Gen von M-MLV auf einem Plasmid exprimiert

Wirkungs- und Qualitätskontrolle
SDS-PAGE-Reinheitsgrad, Endodesoxyribonuklease-, Exodesoxyribonuklease- und Ribonuklease-Assays sowie Ausbeute und Länge von cDNA

Definition einer Einheit
Eine Einheit von M-MLV-RT ist die Enzymmenge, die benötigt wird, um in 10 Minuten bei 37 °C mit Poly(A)-Oligo(dT)25 als Template/Primer 1 nmol Desoxyribonukleotid in säurefällbares Material einzubauen.

Reaktionsbedingungen pro Einheit
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)25, 0,1 mg/ml BSA und Enzym in 50 µl für 10 min bei 37 °C.

Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.

Specifications
EndprodukttypcDNA (Erststrang)
FormatRörchen
Anzahl Reaktionen200 Reaktionen
Optimale Reaktionstemperatur37 °C
Menge200 Reaktionen; 40.000 Einheiten
ReaktionsformatSeparate Komponenten
ReagenztypReverse Transkription
Reverse TranskriptaseM-MLV
Ribonuklease-H-AktivitätJa
VersandbedingungNasseis
Größe (Endprodukt)Bis 7 kb
AusgangsmaterialRNA
VerfahrenReverse Transkription
Konzentration200 U/μl
Reaktionsgeschwindigkeit50 min
Unit SizeEach
Inhalt und Lagerung

• M-mLV RT, 200 μl (200 E/μl)
• 5X-Erststrangpuffer, 1 ml
• DTT, 500 μl (100 mM)

Lagerung bei –20 °C.

Häufig gestellte Fragen (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.

Zitierungen und Referenzen (4)

Zitierungen und Referenzen
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