Taq Polymerase Toyobo

Photos of Taq Polymerase Toyobo

De Novo Gene Expression And Antisense Inhibition In Cultured …
Taq polymerase (Toyobo), were performed at 58 jC as the annealing temperature. After a 1.2-kbp fragment detectable in the PCR mixture by electrophoresis was cloned into a TA- … Fetch Full Source

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Blend Taq-Plus-
Concentration: Blend Taq-Plus- 2.5 units/ul Anti-Taq DNA polymerase antibody 0.5 ug/ul Toyobo suggests >70 ¥ melting temperature of primer (Tm) for long target (>6kb). … Access Full Source

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Involvement Of The Multidomain Regulatory Protein XynR In …
Reverse primer, 1 M deoxynucleoside triphosphates, 2.5 U of rTaq polymerase (Toyobo Co. Ltd., Osaka, Japan), and 10 lof10 rTaq buffer (Toyobo Co. … Access Full Source

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Ampdirect ® Plus Procedure
2 For use of Hot Start Taq DNA Polymerase, we recommend the use of a combination of anti-Taq antibody and Taq DNA Polymerase (e.g. TaKaRa Ex Taq ® Hot Start Version (Takara Bio Inc.), Blend Taq. TM-Plus- (Toyobo Co., LTD.), or Platinum … Content Retrieval

Taq Polymerase Toyobo Images

PHYLOGENETIC PLACEMENT, GENOME SIZE, AND GC CONTENT OF THE …
Primers based on plant actin sequences, and Taq polymerase (Toyobo). Degenerate primer sequences were as follows: forward primer, 5¢-ATGACGCARATHATGTTYGAR; reverse … Read Content

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Molecular Systematics Of Lilium And Allied Genera (Liliaceae …
The matK gene was amplified using the Taq polymerase (Toyobo, Tokyo, Japan) and universal primers, trnK 3914FM and trnK-2R of Johnson & Soltis (1995). … Get Doc

Taq Polymerase Toyobo

A Comparative Study Of Thermomyces Lanuginosus Strains On …
0.2 U of Blend Taq Plus DNA polymerase (Life Science Depart-ment, Toyobo Co., LTD, Japan) and recombinant Taq DNA polymerase (Life Science Department, Toyobo Co., LTD, Japan) … Fetch Content

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Materials And Methods
The reaction buffer supplied with the Blend Taq DNA polymerase (Toyobo). Total RNA was isolated from frozen mycelial mats, according to the method described by Masunaka et al.28. … Get Content Here

Taq Polymerase Toyobo

Sp.nov.,the Causative Agent Of Bacterial Haemorrhagic Ascites …
Were amplified using PCR (Saiki et al., 1988) with Taq polymerase(Toyobo)andtheuniversalprimerpairof20F (5«-AGAGTTTGATCCTGGCTCAG-3«)and1500R(5« … Fetch Here

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Expression Of G Protein-Coupled Receptor-30, A G Protein …
PCR was performed using Taq polymerase (Toyobo)underthefollowingconditions:95Cfor5min;95Cfor60sec, 55 C for 60 sec, 72 C for 60 sec, 35 cycles. … View Document