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TaKaRa gxl taq polymerase
Gxl Taq Polymerase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gxl taq polymerase/product/TaKaRa
Average 94 stars, based on 5 article reviews
Price from $9.99 to $1999.99
gxl taq polymerase - by Bioz Stars, 2020-04
94/100 stars

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DNA Extraction:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Paragraph title: DNA Extraction and PCR Amplification ... Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI).

Clone Assay:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Amplification:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: Identification of the replication region in pBCNF5603, a bacteriocin-encoding plasmid, in the enterotoxigenic Clostridium perfringens strain F5603
Article Snippet: The primers used for amplification of the putative replication regions are listed in Additional file : Table S1. .. In these PCR reactions, each PCR mixture contained 1 μl of template DNA, 0.4 μl of GXL Taq polymerase (TAKARA BIO, Otsu, Japan), 3 μl of 2 mM NTPs, 10 μl of PCR buffer, and 2 μl of each primer pair (1 μM final concentration).

Agarose Gel Electrophoresis:

Article Title: Unraveling the spectrum of KIT mutations in gastrointestinal stromal tumors: An Indian Tertiary Cancer Center Experience
Article Snippet: KIT polymerase chain reaction In brief, PCR reaction was performed in 20 μl containing 100 ng of template DNA, 4 μL of × 5 PCR buffer, 0.7 μL (10 pmol/μL) of each primer,[ ] 1.6 μL of 10 mM deoxynucleoside triphosphates, and 0.4 μL of GXL Taq polymerase (Takara, Clontech). .. The PCR conditions were: 95°C for 15 min followed by 40 cycles of 95°C for 30 s, 56°C for 1 min, 72°C for 1 min, and final extension at 72°C for 10 min. PCR products were analyzed in 1.5% agarose gel and subjected to purification using EXO-SAP IT (USB, Affymetrix).

Polymerase Chain Reaction:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: Unraveling the spectrum of KIT mutations in gastrointestinal stromal tumors: An Indian Tertiary Cancer Center Experience
Article Snippet: .. KIT polymerase chain reaction In brief, PCR reaction was performed in 20 μl containing 100 ng of template DNA, 4 μL of × 5 PCR buffer, 0.7 μL (10 pmol/μL) of each primer,[ ] 1.6 μL of 10 mM deoxynucleoside triphosphates, and 0.4 μL of GXL Taq polymerase (Takara, Clontech). .. The PCR conditions were: 95°C for 15 min followed by 40 cycles of 95°C for 30 s, 56°C for 1 min, 72°C for 1 min, and final extension at 72°C for 10 min. PCR products were analyzed in 1.5% agarose gel and subjected to purification using EXO-SAP IT (USB, Affymetrix).

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: Identification of the replication region in pBCNF5603, a bacteriocin-encoding plasmid, in the enterotoxigenic Clostridium perfringens strain F5603
Article Snippet: .. In these PCR reactions, each PCR mixture contained 1 μl of template DNA, 0.4 μl of GXL Taq polymerase (TAKARA BIO, Otsu, Japan), 3 μl of 2 mM NTPs, 10 μl of PCR buffer, and 2 μl of each primer pair (1 μM final concentration). .. PCR reactions were performed under conditions previously described [ ].

Construct:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Gene trees were constructed based on the nucleotide sequence of cytochrome-b gene by the methods of maximum likelihood (ML), neighbor joining (NJ) and maximum parsimony (MP) methods using Mega 7 software ( ). p -distance was also calculated using the above software.

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Gene trees were constructed based on the nucleotide sequence of cytochrome-b gene by the methods of maximum likelihood (ML), neighbor joining (NJ) and maximum parsimony (MP) methods using Mega 7 software ( ). p -distance was also calculated using the above software.

Purification:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: Unraveling the spectrum of KIT mutations in gastrointestinal stromal tumors: An Indian Tertiary Cancer Center Experience
Article Snippet: KIT polymerase chain reaction In brief, PCR reaction was performed in 20 μl containing 100 ng of template DNA, 4 μL of × 5 PCR buffer, 0.7 μL (10 pmol/μL) of each primer,[ ] 1.6 μL of 10 mM deoxynucleoside triphosphates, and 0.4 μL of GXL Taq polymerase (Takara, Clontech). .. The PCR conditions were: 95°C for 15 min followed by 40 cycles of 95°C for 30 s, 56°C for 1 min, 72°C for 1 min, and final extension at 72°C for 10 min. PCR products were analyzed in 1.5% agarose gel and subjected to purification using EXO-SAP IT (USB, Affymetrix).

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: Identification of the replication region in pBCNF5603, a bacteriocin-encoding plasmid, in the enterotoxigenic Clostridium perfringens strain F5603
Article Snippet: In these PCR reactions, each PCR mixture contained 1 μl of template DNA, 0.4 μl of GXL Taq polymerase (TAKARA BIO, Otsu, Japan), 3 μl of 2 mM NTPs, 10 μl of PCR buffer, and 2 μl of each primer pair (1 μM final concentration). .. After confirming PCR amplification, each PCR product was clarified using the QIAquick PCR purification kit (QIAGEN, Tokyo, Japan) and then digested with restriction enzymes: AvrII/BstBI (NEB, Tokyo, Japan) or AvrII/HpaI (NEB, Tokyo, Japan) for the pCP13-homologous putative replication region on pBCNF5603; SpeI/SnaBI (NEB, Tokyo, Japan) for the pIP404-homologous putative replication region on pBCNF5603; and BsmI/PflMI (NEB, Tokyo, Japan) for the putative rep region on pCP8533S12 (Fig. ).

Concentration Assay:

Article Title: Identification of the replication region in pBCNF5603, a bacteriocin-encoding plasmid, in the enterotoxigenic Clostridium perfringens strain F5603
Article Snippet: .. In these PCR reactions, each PCR mixture contained 1 μl of template DNA, 0.4 μl of GXL Taq polymerase (TAKARA BIO, Otsu, Japan), 3 μl of 2 mM NTPs, 10 μl of PCR buffer, and 2 μl of each primer pair (1 μM final concentration). .. PCR reactions were performed under conditions previously described [ ].

Sequencing:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: .. Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: Identification of the replication region in pBCNF5603, a bacteriocin-encoding plasmid, in the enterotoxigenic Clostridium perfringens strain F5603
Article Snippet: Identification of the replication region in the bacteriocin-encoding plasmid pBCNF5603 Sequence analysis with BLAST indicated that pBCNF5603 mainly consists of two regions: a pCP13-like ORF region and a pIP404-like bacteriocin region (described in the results section). .. In these PCR reactions, each PCR mixture contained 1 μl of template DNA, 0.4 μl of GXL Taq polymerase (TAKARA BIO, Otsu, Japan), 3 μl of 2 mM NTPs, 10 μl of PCR buffer, and 2 μl of each primer pair (1 μM final concentration).

Plasmid Preparation:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Mitochondrial fragments including D-loop region (300∼500 bp) were amplified and purified by the above methods, and were cloned into pUC118 vector using Mighty cloning kit (TaKaRa) with competent cell DH5α (Ecos, Nippon gene) according to the manufactures’ instructions.

Article Title: Identification of the replication region in pBCNF5603, a bacteriocin-encoding plasmid, in the enterotoxigenic Clostridium perfringens strain F5603
Article Snippet: Paragraph title: Identification of the replication region in the bacteriocin-encoding plasmid pBCNF5603 ... In these PCR reactions, each PCR mixture contained 1 μl of template DNA, 0.4 μl of GXL Taq polymerase (TAKARA BIO, Otsu, Japan), 3 μl of 2 mM NTPs, 10 μl of PCR buffer, and 2 μl of each primer pair (1 μM final concentration).

Software:

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Gene trees were constructed based on the nucleotide sequence of cytochrome-b gene by the methods of maximum likelihood (ML), neighbor joining (NJ) and maximum parsimony (MP) methods using Mega 7 software ( ). p -distance was also calculated using the above software.

Article Title: The Distributions and Boundary of Two Distinct, Local Forms of Japanese Pond Frog, Pelophylax porosus brevipodus, Inferred From Sequences of Mitochondrial DNA
Article Snippet: Mitochondrial cytochrome b and nuclear SOX3 fragments were amplified in 50 μl solution including 1.0 μl of DNA solution, 0.2 μl GXL Taq polymerase (TaKaRa), 5 μl of 10× Buffer, 4 μl of 2.5 mM dNTP, and 1 μl of 12.5 mM primers at 98°C for 5 s followed by 30 cycles of 98°C 10 s, 64°C for 40 s, and 72°C for 60 s. The amplified product was purified using GFX PCR DNA and Gel band purification kit (GE Healthcare), and was used for nucleotide sequence determination with 3130XL sequencing machine (ABI). .. Gene trees were constructed based on the nucleotide sequence of cytochrome-b gene by the methods of maximum likelihood (ML), neighbor joining (NJ) and maximum parsimony (MP) methods using Mega 7 software ( ). p -distance was also calculated using the above software.

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    TaKaRa primestar gxl taq polymerase
    Primestar Gxl Taq Polymerase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primestar gxl taq polymerase/product/TaKaRa
    Average 99 stars, based on 4 article reviews
    Price from $9.99 to $1999.99
    primestar gxl taq polymerase - by Bioz Stars, 2020-04
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    TaKaRa pcr amplification
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    Average 99 stars, based on 611 article reviews
    Price from $9.99 to $1999.99
    pcr amplification - by Bioz Stars, 2020-04
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