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MMLV RT/ 重组白血病病毒反转录酶
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MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
MMLV RT/ 重组白血病病毒反转录酶
产品编号：ENZ-310
产品规格：2500U/10000U/50000U
Description MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. Source Recombinant E. coli strain. Physical Appearance Sterile Filtered clear solution （200 U/μl）. Concentration 200 units/ml. Formulation 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. Stability Stable for 5 days at 10°C, for longer period of time store at -20°C.
Please prevent freeze-thaw cycles. Applications 1. 1st strand cDNA synthesis.
2. Primer extension.
3. RT-PCR. Unit Definition One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. 5X Reaction Buffer 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. Usage Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
产品规格：2500U/10000U/50000U
| Description | MMLV （Moloney Murine Leukemia Virus） Reverse Transcriptase is a DNA polymerase that synthesizes a complementary DNA strands from single-stranded RNA, DNA, or an RNA-DNA hybrid as a template. This recombinant enzyme was purified from E.coli, which carried a modified MMLV-RT gene. Compared to AMV Reverse Transcriptase, this enzyme has a much weaker 5＇ - 3＇ ribonuclease H activity, which allows the syntesis of longer cDNAs （>7kb）. |
| Source | Recombinant E. coli strain. |
| Physical Appearance | Sterile Filtered clear solution （200 U/μl）. |
| Concentration | 200 units/ml. |
| Formulation | 50mM Tris-HCl, 0.1M NaCl, 0.1% Triton X-100, 2mM DTT, 0.1mM EDTA ａnd 50% glycerol. |
| Stability | Stable for 5 days at 10°C, for longer period of time store at -20°C. Please prevent freeze-thaw cycles. |
| Applications | 1. 1st strand cDNA synthesis. 2. Primer extension. 3. RT-PCR. |
| Unit Definition | One unit is defined as the amount of enzyme required to catalyze the incorporation of 1nmol of deoxyribonucleotide into acid-insoluble forms in 10 minutes at 37oC, using poly（A）-oligo（dT）12-18 as the template-primer. Standard cDNA Synthesis Conditions50mM Tris-HCl （pH8.3）, 75mM KCl, 3mM MgCl2, 10mM DTT, 1.0mM each dATP, dGTP, dCTP, ａnd dTTP, 0.2 mg radom hexamer,1-5mg RNA, 200units M-MLV RT. The reaction volume was 20ml ａnd the incubation was 45 min at 42oC. |
| 5X Reaction Buffer | 250mM Tris-HCl （pH8.3）, 375mM KCl, 15mM MgCl2, ａnd 50mM DTT. |
| Usage | Prospec＇s products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals. |
