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NotI (10 U/µL)- 300 units – ER0591
Thermo Scientific conventional restriction endonucleases are a large collection of high quality restriction enzymes, optimized to work in one of the buffers of the Five Buffer System. In addition, the universal Tango buffer is provided for convenience in double digestions. All of the enzymes exhibit 100% activity in the recommended buffer and reaction conditions. To ensure consistent performance, Thermo Scientific restriction enzyme reaction buffers contain premixed BSA, which enhances the stability of many enzymes and binds contaminants that may be present in DNA preparations.
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PacI – ER2201
Features
• Superior quality—stringent quality control and industry leading manufacturing process
• Convenient color-coded Five Buffer System
• Includes universal Tango buffer for double-digestions
• BSA premixed in reaction buffers
• Wide selection of restriction endonuclease specificities
Applications
• Molecular cloning
• Restriction site mapping
• Genotyping
• Southern blotting
• Restriction fragment length polymorphism (RFLP)
• SNP
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PagI (BspHI) – ER1281
5′ T ↓ C A T G A 3′ 3′ A G T A C ↑ T 5′ Thermo Scientific PagI (BspHI) restriction enzyme recognizes T^CATGA sites and cuts best at 37°C in O buffer (isoschizomers: BspHI, CciI, RcaI). See Reaction Conditions for Restriction Enzymes for a table of enzyme activity, conditions for double digestion,…
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PdmI (XmnI) – ER1531
Molecular cloning•
Restriction site mapping•
Genotyping•
Southern blotting•
Restriction fragment length polymorphism (RFLP)•
SNP•
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PfeI (TfiI) (10 U/µL) (500 Units) – ER1781
Applications
• Molecular cloning
• Restriction site mapping
• Genotyping
• Southern blotting
• Restriction fragment length polymorphism (RFLP)
• SNP
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Ppu21I (BsaAI) – ER1971
5′ Y A C ↓ G T R 3′ 3′ R T G ↑ C A Y 5′ Thermo Scientific Ppu21I (BsaAI) – ER1971 restriction enzyme recognizes YAC^GTR sites and cuts best at 30°C in its own unique buffer (isoschizomers: BsaAI, BstBAI). See Reaction Conditions for Restriction Enzymes for a table of enzyme activity, conditions for double…
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Proteinase K- 20mg/ml – 1ml
Proteinase K from Parengyodontium album (Tritirachium album) is a subtilisinrelated serine protease. It is a broad spectrum endopeptidase with very high specific activity. It is widely used for digestion of proteins, including DNases and RNases, during nucleic acid preparations without compromising integrity of isolated DNA or RNA. Proteinase K is active under wide range of…
675,000 تومان
PstI (10 U/µL) – ER0611 – 3,000 units
Storage Buffer
PstI is supplied in: 10 mM Tris-HCl (pH 7.4 at 25°C),
200 mM NaCl, 1 mM DTT, 0.1 mM EDTA,
0.15% Triton X-100, 0.2 mg/mL BSA and 50% glycerol.
Recommended Protocol for Digestion
• Add:
nuclease-free water 16 μL
10X Buffer O 2 μL
DNA (0.5-1 μg/μL) 1 μL
PstI 0.5-2 μL
• Mix gently and spin down for a few seconds.
• Incubate at 37°C for 1-16 hours.
The digestion reaction may be scaled either up or down.
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RevertAid First Strand cDNA Synthesis Kit Fermentas
• Full-length first strand cDNA up to 13 kb
• Optimum reaction temperature 42°C
• Complete kit—all the components for the RT reaction are included
Applications
• First strand cDNA synthesis for RT-PCR and RT-qPCR
• Construction of full length cDNA libraries
• Antisense RNA synthesis
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Ribonuclease A DNase and Protease Free 20mg/ml
The working concentration of RNase A is 1‐100μg/ml,
depending on the application.
The enzyme is active under a wide range of reaction
conditions. At low salt concentrations (to 100mM NaCl),
RNase A cleaves single‐stranded and double‐stranded RNA
as well the RNA strand in RNA‐DNA hybrids. However, at
NaCl concentrations of 0.3M or higher, RNase A specifically
cleaves single‐stranded RNA.
Applications
Plasmid and genomic DNA preparation.
Removal of RNA from recombinant protein
preparations.
Ribonuclease protection assays .
Mapping single‐base mutations in DNA or RNA.
795,000 تومان
SacI – ER1132
• Superior quality—stringent quality control and industry leading manufacturing process
• Convenient color-coded Five Buffer System
• Includes universal Tango buffer for double-digestions
• BSA premixed in reaction buffers
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SalI (10 U/µL) – ER0641
SalI is supplied in: 10 mM Tris-HCl (pH 7.4 at 25°C),
100 mM KCl, 1 mM DTT, 0.1 mM EDTA, 0.2 mg/mL BSA
and 50% glycerol.
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Sinnaclon First Strand cDNA Synthesis Kit-50T
Kit Components(50 reactions)
M‐MuLV Reverse Transcriptase (200u/μl) 5000u
RNase Inhibitor (40u/μl) 1000u
5X Buffer M‐MuLV 200 μl
DTT (0.1M) 50 μl
10mM dNTPs mix 100 μl
Oligod(T)18 (40μM) 50 μl
Random hexamer (50ng/μl) 50 μl
DEPC‐treated water 1 ml
6,500,000 تومان
















