| Identification | Back Directory | [Name]
DNA polymerase | [CAS]
9012-90-2 | [Synonyms]
Eta2
HHKF
KLENOW
MTP™
EC 2.7.7.7
IUB: 2.7.7.7
POLYMERASE I
KLENOW ENZYME
PhyScript Taq
Klenowfragment
DNA POLYMERASE
RAD30 homolog B
DNA POLYMERASE I
T4 DNA POLYMERASE
TAQ DNA POLYMERASE
DNA POLYMERASE, T4
DNA POLYMERASE, TAQ
REDTaqSuperPak™
KORNBERG POLYMERASE
TAQ BUFFER WITH KCL
TAKARA TAQ POLYMERASE
EXO- KLENOW POLYMERASE
RED TAQ DNA POLYMERASE
Q-BIOTAQ DNA POLYMERASE
DNA POLYMERASE I, KLENOW
ARROW TAQ(TM) POLYMERASE
TAKARA EX TAQ POLYMERASE
MTP(R) TAQ DNA POLYMERASE
TAQ BUFFER WITH (NH4)2SO4
MTP(TM)TAQ DNA POLYMERASE
10X Taq Buffer(with Mg2+)
TAQ DNA POLYMERASE DNA-FREE
JUMPSTART(R) TAQ READYMIX(R)
JUMPSTART TAQ DNA POLYMERASE
REDTAQ GENOMIC DNA POLYMERASE
TAQ BUFFER WITH KCL AND MGCL2
JUMPSTART(TM) TAQ READYMIX(TM)
JUMPSTART REDTAQ DNA POLYMERASE
JUMPSTART(TM) TAQ DNA POLYMERASE
T4 DNA POLYMERASE, LIC-QUALIFIED
DNA POLYMERASE I, LARGE FRAGMENT
DNA POLYMERASE 1, LARGE FRAGMENT
DNA POLYMERASE 1, KLENOW FRAGMENT
TAQ DNA POLYMERASE CUSTOM PACKAGE
DNA POLYMERASE 1, KLENOV FRAGMENT
10X Taq Buffer(with Mg2+), for PCR
DNA POLYMERASE I (KLENOW FRAGMENT)
TAQ BUFFER WITH (NH4)2SO4 AND MGCL2
KLENOW FRAGMENT OF DNA POLYMERASE I
TAQ DNA POLYMERASE (NATIVE, WITH BSA)
TAQ DNA POLYMERASE (NATIVE, WITHOUT BSA)
DNA POLYMERASE I LARGE (KLENOW) FRAGMENT
taq dna polymerase from thermus aquaticus
Nucleotidyltransferase, deoxyribonucleate
JumpStart? REDTaq? ReadyMix? Reaction Mix
dna polymerase T4 from E. coli 71-18/ ptl43W
DNA Polymerase Alpha from Human, Recombinant
REDTAQ GENOMIC DNA POLYMERASE, BR，2-5u/ul，99%
DNA POLYMERASE I, KLENOW FRAGMENT FROM*E . COLI
TAQ-T THERMUS AQUATICUS DNA POLYMERASE, MODIFIED
Anti-POLI, C-Terminal antibody produced in rabbit
dna polymerase I from E.coli lysogen*carrying bac
T4 dna polymerase from phage T4*infected escheric
taq dna polymerase with 10X reaction*buffer conta
DNA POLYMERASE I LARGE FRAGMENT (KLENOW FRAGMENT)
dna polymerase I from E. coli lysogenic for nm 964
T4 DNA POLYMERASE FROM PHAGE T4INFECTED ESCHERICHI
TAQ DNA POLYMERASE WITH 10X REACTIONBUFF ER WITHOUT
DNA POLYMERASE I FROM E.COLI LYSOGEN*CAR RYING BACTE
dna polymerase t4 from escherichia coli 71-18/ptl43w
Taq DNA Polymerase(with 10x PCR buffer,Premixed MgCl2)
dna polymerase i, klenow fragment from escherichia coli
KLENOW ENZYME, E. COLI, FOR MOL. BIOL., DRY ICE, 100 U*
DNA POLYMERASE I FROM E. COLI LYSOGENIC FOR NM 964, 250 U*
dna polymerase i from escherichia coli lysogenic for nm 964
DNA POLYMERASE I LARGE (KLENOW) FRAGMENT, EXONUCLEASE MINUS
DNA Polymerase T4 from Escherichia coli 71-18/pTL43W,T4-DNA-Polymerase
DNA POLYMERASE I LARGE FRAGMENT, EXONUCLEASE MINUS (KLENOW FRAGMENT, EXO-)
DEOXYNUCLEOSIDE-TRIPHOSPHATE:DNA DEOXYNUCLEOTIDYLTRANSFERASE [DNA-DIRECTED]
DNA Polymerase I from Escherichia coli lysogenic for NM 964,Kornberg Polymerase | [EINECS(EC#)]
232-741-2 | [Molecular Formula]
NULL | [MDL Number]
MFCD00283091 |
| Hazard Information | Back Directory | [Uses]
For routine PCR amplifications REDTaq? DNA Polymerase has been used in polymerase chain reaction (PCR) and reverse transcription-polymerase chain reaction (RT-PCR) analysis. | [Uses]
REDTaq? Genomic DNA Polymerase has been used as a component of the polymerase chain reaction (PCR) mix for PCR amplification. It has also been used as a component of the preamplification mix for PCR in amplified fragment length polymorphism (AFLP) analysis of Fusarium oxysporum sp. isolates. | [Uses]
Taq DNA Polymerase from Thermus aquaticus has been used in the process of DNA extraction (during gene amplification and sequencing). It has been used in genotyping. It has also been used in polymerase chain reaction (PCR) to study the constitutive production of epithelial neutrophil activating peptide 78 (ENA-78) and interleukin-8 (IL-8). | [General Description]
Klenow enzyme is the large, C-terminal fragment (Mr 76,000) of E.coli DNA polymerase I, which can be obtained by subtilisin treatment of intact DNA polymerase I. It retains the 5′→3′ polymerase and the 3′→5′ exonuclease activities of intact DNA polymerase I, but lacks the 5′→3′ exonuclease activity of the native enzyme. The enzyme catalyzes the addition of mononucleotides from deoxynucleoside-5′-triphosphates to the 3′-hydroxyl terminus of a primer/template DNA. This property is used to synthesize DNA complementary to single-stranded DNA templates.
Klenow Enzyme is formed by subtilisin treatment of DNA polymerase I. | [Biochem/physiol Actions]
Taq polymerase catalyzes oligonucleotide primer-driven, DNA template dependent incorporation of dNTPs into complimentary DNA strands. It displays both 5′ to 3′ polymerase and exonuclease activities. |
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| Company Name: |
Sigma-Aldrich
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021-61415566 800-8193336 |
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https://www.sigmaaldrich.cn |
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