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Recommended products

T4 DNA Ligase (Rapid)
CAT NO./ID L6030-HC-L
T4 DNA Ligase (Rapid)
240,000 U of T4 DNA Ligase (600,000 U/mL) 2x Rapid Ligation Buffer and 10x T4 DNA Ligase Buffer
719,00 €
T7 DNA Ligase (900,000 U)
CAT NO./ID L6020L
T7 DNA Ligase (900,000 U)
900,000 U of T7 DNA Ligase (3,000,000 U/mL) and 2x Rapid Ligation Buffer
450,00 €
T4 DNA Polymerase (exo) (2000 U)
CAT NO./ID P7080L
T4 DNA Polymerase (exo) (2000 U)
2000 U of T4 DNA Polymerase (3000 U/mL) and 10x Blue Buffer. Storage temperature: –25°C to –15°C
474,00 €
T4 DNA Ligase MBG (2500 U)
CAT NO./ID EN11-250
T4 DNA Ligase MBG (2500 U)
5 x 100 μL of T4 DNA Ligase 5U/ μL, 5 x 200 μL 10x T4 Ligation Buffer, 5 x 80 μL of ATP Solution (25mM), 5 x 200 μL of 50% PEG Solution. Storage temperature: Keep at -20°C.
179,00 €
Klenow Fragment (2500 U)
CAT NO./ID P7060L
Klenow Fragment (2500 U)
2500 U of Klenow Fragment (0.5 mL at 5000 U/mL) and 10x Blue Buffer (1 x 1.5 mL)
450,00 €
Saltonase (5000 U)
CAT NO./ID EN32-050
Saltonase (5000 U)
20 µL x 250 U/µL. Storage temperature: -20°C without a defrost cycle; -80°C for long storage. Stable at -20°C for at least 12 months. No loss in activity was observed after 8 weeks of incubation at 37°C.
134,00 €
End-Repair Mix (low concentration)
CAT NO./ID Y9140-LC-L
End-Repair Mix (low concentration)
For 200 low-concentration DNA reactions. End-Repair Mix 1X (0.20 mL), 10X End-Repair Buffer (1 x 1.5 mL) and 1 mM dNTP solution (0.5 mL).
474,00 €
AllTaq PCR Core Kit (250 U)
CAT NO./ID 203123
AllTaq PCR Core Kit (250 U)
50 µl AllTaq Polymerase (5 U/µl), 1.2 ml AllTaq PCR Buffer (5x), 55 µl dNTP Mix (10 mM each), 200 µl Template Tracer (25x), 50 µl Master Mix Tracer (125x), 2 ml Q-Solution (5x), 1.2 ml MgCl2 (25 mM), 1.9 ml RNase-Free Water
194,00 €
Taq DNA Polymerase (250 U)
CAT NO./ID 201203
Taq DNA Polymerase (250 U)
250 units Taq DNA Polymerase, 10x PCR Buffer, 10x CoralLoad PCR Buffer, 5x Q-Solution, 25 mM MgCl2
163,00 €
RNase A (17,500 U)
CAT NO./ID 19101
RNase A (17,500 U)
2.5 ml (100 mg/ml; 7000 units/ml, solution) Unit definition: That amount of enzyme causing the hydrolysis of RNA at a rate such that k (velocity constant) equals unity (Kunitz units) at 25°C and pH 5.0.
292,00 €
HotStarTaq DNA Polymerase (250 U)
CAT NO./ID 203203
HotStarTaq DNA Polymerase (250 U)
250 units HotStarTaq DNA Polymerase, 10x PCR Buffer, 5x Q-Solution, 25 mM MgCl2
193,00 €
Omniscript RT Kit (50)
CAT NO./ID 205111
Omniscript RT Kit (50)
For 50 reverse-transcription reactions: 200 units Omniscript Reverse Transcriptase, 150 µl 10x Buffer RT, 100 µl dNTP Mix (contains 5 mM each dNTP), 1.1 ml RNase-free water
331,00 €
RNase-Free DNase Set (50)
CAT NO./ID 79254
RNase-Free DNase Set (50)
1500 Kunitz units RNase-free DNase I, RNase-free Buffer RDD, and RNase-free water for 50 RNA minipreps
124,00 €
QIAGEN Protease (7.5 AU)
CAT NO./ID 19155
QIAGEN Protease (7.5 AU)
7.5 Anson units per vial (lyophilized)
103,00 €
QIAGEN Proteinase K (2 ml)
CAT NO./ID 19131
QIAGEN Proteinase K (2 ml)
2 ml (>600 mAU/ml, solution)
105,00 €

Ligation Calculator

This tool determines the mass of insert needed for various inserts:vector molar ratios within the range suitable for typical ligation reactions.

icon_0330_cc_gen_calculator-s

 

Required insert DNA mass [g] = vector DNA mass [g] x {insert DNA length / vector DNA length} x desired insert to vector molar ratio

Notes: Desired ratio is one from set { 1, 2, 3, 5 ,7}

Insert length should be smaller than vector length

First, the insert and vector DNA is digested using restriction endonucleases to create DNA fragments with sticky (or blunt) ends. Next, the desired DNA fragments are isolated and subsequently joined followed by treatment with DNA ligase. Finally, the resulting intact vector is transformed into competent E. coli cells, and transformants are identified through suitable genetic selection methods. 

 

Want to know more about the step-by-step process of DNA ligation and its typical reaction? Learn more.

Discover enzymes that you can use for ligating DNAs.