bamhi recognition site (TaKaRa)
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TaKaRa
bamhi recognition site
Bamhi Recognition Site, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 14678 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bamhi+recognition+site/BamH+I/us12600991-473-27-37
Average 99 stars, based on 14678 article reviews
Bamhi Recognition Site, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 14678 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bamhi+recognition+site/BamH+I/us12600991-473-27-37
Average 99 stars, based on 14678 article reviews
bamhi recognition site - by Bioz Stars,
2026-09
99/100 stars
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Transcription Assay:Article Title: The Homeodomain Transcription Factor Xvent-2 Mediates Autocatalytic Regulation of BMP-4 Expression in XenopusEmbryos Article Snippet: .. Yeast Transcriptional Assay (28)—Xvent-1 and Xvent-2 were integrated in-frame into the Bacteria:Article Title: The Homeodomain Transcription Factor Xvent-2 Mediates Autocatalytic Regulation of BMP-4 Expression in XenopusEmbryos Article Snippet: .. Yeast Transcriptional Assay (28)—Xvent-1 and Xvent-2 were integrated in-frame into the Plasmid Preparation:Article Title: The Homeodomain Transcription Factor Xvent-2 Mediates Autocatalytic Regulation of BMP-4 Expression in XenopusEmbryos Article Snippet: .. Yeast Transcriptional Assay (28)—Xvent-1 and Xvent-2 were integrated in-frame into the Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Article Title: Genetically modified microorganism for production of aspartic acid and downstream metabolites from aspartic acid as target substance, and method for producing target substance using same Article Snippet: Hereinafter, the procedures therefor are shown. (1) Preparation of Gene-Deficient Strain (Corynebacterium glutamicum Strain ATCC13032 ΔldhΔsdhΔpoxB) At first, a SacB gene fragment was amplified by the PCR method using plasmid pNIC-Bsa4 (Source BioScience) serving as a template, and a pair of primers shown in Table 12 below. .. TABLE 12 SEQ Primer ID name Sequence and description NO: Primer 5′-GGGGAAGCTTGACGTCCACATATACCTGCC-3′ 14 F1 Underlined part: HindIII- recognition site Primer 5′-ATTCGGATCCGTATCCACCTTTAC-3′ 15 R1 Underlined part: Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Polymerase Chain Reaction:Article Title: Novel single nucleotide polymorphisms in the bovine leukemia virus genome are associated with proviral load and affect the expression profile of viral non-coding transcripts. Article Snippet: Bovine leukemia virus (BLV) infects bovine B-cells and causes malignant lymphoma, resulting in severe economic losses in the livestock industry.. To control the spread of BLV, several studies have attempted to clarify the molecular mechanisms of BLV pathogenesis, but the details of the mechanism are still enigmatic.. Currently, viral non-coding RNAs are attracting attention as a novel player for BLV pathogenesis because these transcripts can evade the host immune response and are persistently expressed in latent infection. Amplification:Article Title: Novel single nucleotide polymorphisms in the bovine leukemia virus genome are associated with proviral load and affect the expression profile of viral non-coding transcripts. Article Snippet: Bovine leukemia virus (BLV) infects bovine B-cells and causes malignant lymphoma, resulting in severe economic losses in the livestock industry.. To control the spread of BLV, several studies have attempted to clarify the molecular mechanisms of BLV pathogenesis, but the details of the mechanism are still enigmatic.. Currently, viral non-coding RNAs are attracting attention as a novel player for BLV pathogenesis because these transcripts can evade the host immune response and are persistently expressed in latent infection. Article Title: Genetically modified microorganism for production of aspartic acid and downstream metabolites from aspartic acid as target substance, and method for producing target substance using same Article Snippet: Hereinafter, the procedures therefor are shown. (1) Preparation of Gene-Deficient Strain (Corynebacterium glutamicum Strain ATCC13032 ΔldhΔsdhΔpoxB) At first, a SacB gene fragment was amplified by the PCR method using plasmid pNIC-Bsa4 (Source BioScience) serving as a template, and a pair of primers shown in Table 12 below. .. TABLE 12 SEQ Primer ID name Sequence and description NO: Primer 5′-GGGGAAGCTTGACGTCCACATATACCTGCC-3′ 14 F1 Underlined part: HindIII- recognition site Primer 5′-ATTCGGATCCGTATCCACCTTTAC-3′ 15 R1 Underlined part: Clone Assay:Article Title: Novel single nucleotide polymorphisms in the bovine leukemia virus genome are associated with proviral load and affect the expression profile of viral non-coding transcripts. Article Snippet: Bovine leukemia virus (BLV) infects bovine B-cells and causes malignant lymphoma, resulting in severe economic losses in the livestock industry.. To control the spread of BLV, several studies have attempted to clarify the molecular mechanisms of BLV pathogenesis, but the details of the mechanism are still enigmatic.. Currently, viral non-coding RNAs are attracting attention as a novel player for BLV pathogenesis because these transcripts can evade the host immune response and are persistently expressed in latent infection. Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Cloning:Article Title: Novel single nucleotide polymorphisms in the bovine leukemia virus genome are associated with proviral load and affect the expression profile of viral non-coding transcripts. Article Snippet: Bovine leukemia virus (BLV) infects bovine B-cells and causes malignant lymphoma, resulting in severe economic losses in the livestock industry.. To control the spread of BLV, several studies have attempted to clarify the molecular mechanisms of BLV pathogenesis, but the details of the mechanism are still enigmatic.. Currently, viral non-coding RNAs are attracting attention as a novel player for BLV pathogenesis because these transcripts can evade the host immune response and are persistently expressed in latent infection. Derivative Assay:Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Expressing:Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Construct:Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Article Title: Recombinant feline herpesvirus type 1 and polyvalent vaccine using the same Article Snippet: .. That is, a plasmid vector pSal-I (obtained from Dr. T. Miyazawa, Department of Agriculture, Tokyo University) wherein the I fragment as one of the SalI digested DNA fragments of the FHV-1 genome DNA had been integrated was cloned again in a commercial plasmid vector whose Sequencing:Article Title: Genetically modified microorganism for production of aspartic acid and downstream metabolites from aspartic acid as target substance, and method for producing target substance using same Article Snippet: Hereinafter, the procedures therefor are shown. (1) Preparation of Gene-Deficient Strain (Corynebacterium glutamicum Strain ATCC13032 ΔldhΔsdhΔpoxB) At first, a SacB gene fragment was amplified by the PCR method using plasmid pNIC-Bsa4 (Source BioScience) serving as a template, and a pair of primers shown in Table 12 below. .. TABLE 12 SEQ Primer ID name Sequence and description NO: Primer 5′-GGGGAAGCTTGACGTCCACATATACCTGCC-3′ 14 F1 Underlined part: HindIII- recognition site Primer 5′-ATTCGGATCCGTATCCACCTTTAC-3′ 15 R1 Underlined part: DNA Ligation:Article Title: Genetically modified microorganism for production of aspartic acid and downstream metabolites from aspartic acid as target substance, and method for producing target substance using same Article Snippet: Hereinafter, the procedures therefor are shown. (1) Preparation of Gene-Deficient Strain (Corynebacterium glutamicum Strain ATCC13032 ΔldhΔsdhΔpoxB) At first, a SacB gene fragment was amplified by the PCR method using plasmid pNIC-Bsa4 (Source BioScience) serving as a template, and a pair of primers shown in Table 12 below. .. TABLE 12 SEQ Primer ID name Sequence and description NO: Primer 5′-GGGGAAGCTTGACGTCCACATATACCTGCC-3′ 14 F1 Underlined part: HindIII- recognition site Primer 5′-ATTCGGATCCGTATCCACCTTTAC-3′ 15 R1 Underlined part: |
