fati restriction enzyme  (New England Biolabs)


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    Name:
    FatI
    Description:
    FatI 250 units
    Catalog Number:
    r0650l
    Price:
    382
    Size:
    250 units
    Category:
    Restriction Enzymes
    Buy from Supplier


    Structured Review

    New England Biolabs fati restriction enzyme
    FatI
    FatI 250 units
    https://www.bioz.com/result/fati restriction enzyme/product/New England Biolabs
    Average 88 stars, based on 388 article reviews
    Price from $9.99 to $1999.99
    fati restriction enzyme - by Bioz Stars, 2020-04
    88/100 stars

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    Related Articles

    Clone Assay:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: The amplicons were purified and then partially digested with FatI (NEB). .. The ligation mixture was transformed by electroporation into E. coli BW25113 and clones selected on solid LB agar supplemented with 100 μg/ml ampicillin.

    Article Title: ETV1 positively regulates transcription of tumor suppressor ARF
    Article Snippet: ETV1 coding region was amplified from a pool of total cDNA of human fibrosarcoma HT1080 cells and cloned into pBabePuro to create pBabePuroETV1 construct. .. The PCR fragment was cut FatI (New England Biolabs, R0650) and RsaI (New England Biolabs, R0167) and inserted between EcoIRCI (Promega, R6951) and NcoI (New England Biolabs, R0193) sites of pGL3 Basic immediately upstream of the Luciferase gene.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The library ligation mixture was used to transform E. coli JW0941–1 ( ΔsulA ) by electroporation, and clones were selected on LB agar supplemented with 100 μg/ml Ampicillin.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Construction of the shotgun UTI89 genomic DNA expression library Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The library ligation mixture was used to transform E. coli JW0941–1 (ΔsulA ) by electroporation, and clones were selected on LB agar supplemented with 100 μg/ml Ampicillin.

    Amplification:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Paragraph title: Amplification and sub-cloning of fragments from identified genomic regions ... The amplicons were purified and then partially digested with FatI (NEB).

    Article Title: ETV1 positively regulates transcription of tumor suppressor ARF
    Article Snippet: In order to construct ARF luciferase reporter (pARF-luc), a fragment of human genomic DNA was amplified from BAC clone 478M20 (acquired from a library at Roswell Park Cancer Institute) using GCCGCTCCTT CCTTTCCTTG and GATGACTCCT CGGTCGCAGA primers. .. The PCR fragment was cut FatI (New England Biolabs, R0650) and RsaI (New England Biolabs, R0167) and inserted between EcoIRCI (Promega, R6951) and NcoI (New England Biolabs, R0193) sites of pGL3 Basic immediately upstream of the Luciferase gene.

    Article Title: GENETIC DISSECTION OF INTERMALE AGGRESSIVE BEHAVIOR IN BALB/cJ AND A/J MICE
    Article Snippet: Next, we designed PCR primers flanking rs29358506 that amplified a 242 basepair (bp) fragment. .. The concentration of the PCR product was measured using a spectrophotometer, and 2.4 μg of DNA was digested by incubating 2 units of FatI restriction enzyme and buffer (New England Biolabs, Ipswich, MA) at 55°C for 1 hour.

    Construct:

    Article Title: ETV1 positively regulates transcription of tumor suppressor ARF
    Article Snippet: In order to construct ARF luciferase reporter (pARF-luc), a fragment of human genomic DNA was amplified from BAC clone 478M20 (acquired from a library at Roswell Park Cancer Institute) using GCCGCTCCTT CCTTTCCTTG and GATGACTCCT CGGTCGCAGA primers. .. The PCR fragment was cut FatI (New England Biolabs, R0650) and RsaI (New England Biolabs, R0167) and inserted between EcoIRCI (Promega, R6951) and NcoI (New England Biolabs, R0193) sites of pGL3 Basic immediately upstream of the Luciferase gene.

    Incubation:

    Article Title: PAR-TERRA directs homologous sex chromosome pairing
    Article Snippet: First, we digested 3 μg of each 3C library with 4 units of FatI (NEB) for 4 hours at 55 degrees. .. To ligate the universal adaptor to the 3C library, we incubated the 3C library with 200 picomoles universal adaptor and 2 μl T4 DNA Ligase (Enzymatics) in 1X T4 DNA Ligase Buffer (NEB) in a volume of 50 μl for 1 hour at 16°C, then 2 hours at 16°C.

    Luciferase:

    Article Title: ETV1 positively regulates transcription of tumor suppressor ARF
    Article Snippet: .. The PCR fragment was cut FatI (New England Biolabs, R0650) and RsaI (New England Biolabs, R0167) and inserted between EcoIRCI (Promega, R6951) and NcoI (New England Biolabs, R0193) sites of pGL3 Basic immediately upstream of the Luciferase gene. ..

    Expressing:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Construction of the shotgun UTI89 genomic DNA expression library Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Modification:

    Article Title: PAR-TERRA directs homologous sex chromosome pairing
    Article Snippet: Next, we converted the 3C libraries into 4C libraries, using a protocol similar to the modified-4C protocol , but with some modifications. .. First, we digested 3 μg of each 3C library with 4 units of FatI (NEB) for 4 hours at 55 degrees.

    Transformation Assay:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: The amplicons were purified and then partially digested with FatI (NEB). .. The ligation mixture was transformed by electroporation into E. coli BW25113 and clones selected on solid LB agar supplemented with 100 μg/ml ampicillin.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Construction of the shotgun UTI89 genomic DNA expression library Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Derivative Assay:

    Article Title: Epigenetic Control of Cell Cycle-Dependent Histone Gene Expression Is a Principal Component of the Abbreviated Pluripotent Cell Cycle
    Article Snippet: The proximity ligation assay protocol was derived from the previously published chromosome conformation capture (3C) method ( ) with modifications. .. Nuclei were digested with FatI (R0650, New England BioLabs) for 2 h at 55°C and then overnight at 42°C.

    Electroporation:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: The amplicons were purified and then partially digested with FatI (NEB). .. The ligation mixture was transformed by electroporation into E. coli BW25113 and clones selected on solid LB agar supplemented with 100 μg/ml ampicillin.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The library ligation mixture was used to transform E. coli JW0941–1 ( ΔsulA ) by electroporation, and clones were selected on LB agar supplemented with 100 μg/ml Ampicillin.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Construction of the shotgun UTI89 genomic DNA expression library Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The library ligation mixture was used to transform E. coli JW0941–1 (ΔsulA ) by electroporation, and clones were selected on LB agar supplemented with 100 μg/ml Ampicillin.

    Ligation:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: The amplicons were purified and then partially digested with FatI (NEB). .. The ligation mixture was transformed by electroporation into E. coli BW25113 and clones selected on solid LB agar supplemented with 100 μg/ml ampicillin.

    Article Title: Epigenetic Control of Cell Cycle-Dependent Histone Gene Expression Is a Principal Component of the Abbreviated Pluripotent Cell Cycle
    Article Snippet: Nuclei were digested with FatI (R0650, New England BioLabs) for 2 h at 55°C and then overnight at 42°C. .. To reduce the background ligation frequency, the ligation step was carried out in > 80 separate reactions in which each reaction mixture contained 0.5 genomic copy of DNA.

    Article Title: PAR-TERRA directs homologous sex chromosome pairing
    Article Snippet: To purify the DNA, 2 mg Proteinase K was added to the ligation reactions and left at 65°C overnight, then the DNA was cleaned by phenol:cholorform:isoamyl alcohol extraction followed by ethanol precipitation. .. First, we digested 3 μg of each 3C library with 4 units of FatI (NEB) for 4 hours at 55 degrees.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Construction of the shotgun UTI89 genomic DNA expression library Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    other:

    Article Title: GENETIC DISSECTION OF INTERMALE AGGRESSIVE BEHAVIOR IN BALB/cJ AND A/J MICE
    Article Snippet: The FatI restriction enzyme cutting sites (CATG) are indicated in red.

    Polymerase Chain Reaction:

    Article Title: ETV1 positively regulates transcription of tumor suppressor ARF
    Article Snippet: .. The PCR fragment was cut FatI (New England Biolabs, R0650) and RsaI (New England Biolabs, R0167) and inserted between EcoIRCI (Promega, R6951) and NcoI (New England Biolabs, R0193) sites of pGL3 Basic immediately upstream of the Luciferase gene. ..

    Article Title: PAR-TERRA directs homologous sex chromosome pairing
    Article Snippet: First, we digested 3 μg of each 3C library with 4 units of FatI (NEB) for 4 hours at 55 degrees. .. The DNA was then purified using the PCR Purification Kit (Qiagen).

    Article Title: GENETIC DISSECTION OF INTERMALE AGGRESSIVE BEHAVIOR IN BALB/cJ AND A/J MICE
    Article Snippet: .. The concentration of the PCR product was measured using a spectrophotometer, and 2.4 μg of DNA was digested by incubating 2 units of FatI restriction enzyme and buffer (New England Biolabs, Ipswich, MA) at 55°C for 1 hour. .. The digested and undigested PCR products were electrophoresed side-by-side on a 10% polyacrylamide gel and visualized using ethidium bromide staining.

    Subcloning:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: Paragraph title: Amplification and sub-cloning of fragments from identified genomic regions ... The amplicons were purified and then partially digested with FatI (NEB).

    Size-exclusion Chromatography:

    Article Title: GENETIC DISSECTION OF INTERMALE AGGRESSIVE BEHAVIOR IN BALB/cJ AND A/J MICE
    Article Snippet: The PCR cycle was 95°C for 3 min; then 35 cycles of 95°C for 45 sec, 56°C for 30 sec, 72°C for 45 sec; then 72°C for 5 minutes. .. The concentration of the PCR product was measured using a spectrophotometer, and 2.4 μg of DNA was digested by incubating 2 units of FatI restriction enzyme and buffer (New England Biolabs, Ipswich, MA) at 55°C for 1 hour.

    Purification:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. The amplicons were purified and then partially digested with FatI (NEB). ..

    Article Title: Epigenetic Control of Cell Cycle-Dependent Histone Gene Expression Is a Principal Component of the Abbreviated Pluripotent Cell Cycle
    Article Snippet: Nuclei were digested with FatI (R0650, New England BioLabs) for 2 h at 55°C and then overnight at 42°C. .. Cross-links were reversed, and DNA was purified by phenol-chloroform extraction followed by ethanol precipitation.

    Article Title: PAR-TERRA directs homologous sex chromosome pairing
    Article Snippet: First, we digested 3 μg of each 3C library with 4 units of FatI (NEB) for 4 hours at 55 degrees. .. The DNA was then purified using the PCR Purification Kit (Qiagen).

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Construction of the shotgun UTI89 genomic DNA expression library Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Chromatin Immunoprecipitation:

    Article Title: Epigenetic Control of Cell Cycle-Dependent Histone Gene Expression Is a Principal Component of the Abbreviated Pluripotent Cell Cycle
    Article Snippet: Briefly, 4.6 million hES H9 cells were cross-linked and treated as described for ChIP assays. .. Nuclei were digested with FatI (R0650, New England BioLabs) for 2 h at 55°C and then overnight at 42°C.

    Plasmid Preparation:

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    Article Title: High-throughput sequencing of sorted expression libraries reveals inhibitors of bacterial cell division
    Article Snippet: .. Construction of the shotgun UTI89 genomic DNA expression library Purified genomic DNA from E. coli UTI89 was partially digested with FatI (New England Biolabs), a 4-bp-recognition endonuclease that includes the ATG start codon, which would increase the frequency of in-frame ORF ligation to the expression vector compared to other 4-bp-recognition endonucleases. .. The gDNA fragments (1–5 kb range) were gel purified and ligated to pBAD24, which had been prepared by digestion with NcoI (NEB), dephosphorylated with Antarctic Phosphatase (NEB) and verified not to self-ligate by transformation of a vector-only ligation mixture.

    In Situ:

    Article Title: PAR-TERRA directs homologous sex chromosome pairing
    Article Snippet: To perform in-situ ligation, we added 820 μl 10X T4 DNA Ligase Buffer (NEB), 82 μl 10 mg/ml BSA (NEB), 7.61 ml water and 50 μl T4 DNA Ligase (Enzymatics) and rotated for 4 hours at room temperature. .. First, we digested 3 μg of each 3C library with 4 units of FatI (NEB) for 4 hours at 55 degrees.

    Proximity Ligation Assay:

    Article Title: Epigenetic Control of Cell Cycle-Dependent Histone Gene Expression Is a Principal Component of the Abbreviated Pluripotent Cell Cycle
    Article Snippet: Paragraph title: Proximity ligation assay. ... Nuclei were digested with FatI (R0650, New England BioLabs) for 2 h at 55°C and then overnight at 42°C.

    Ethanol Precipitation:

    Article Title: Epigenetic Control of Cell Cycle-Dependent Histone Gene Expression Is a Principal Component of the Abbreviated Pluripotent Cell Cycle
    Article Snippet: Nuclei were digested with FatI (R0650, New England BioLabs) for 2 h at 55°C and then overnight at 42°C. .. Cross-links were reversed, and DNA was purified by phenol-chloroform extraction followed by ethanol precipitation.

    Article Title: PAR-TERRA directs homologous sex chromosome pairing
    Article Snippet: To purify the DNA, 2 mg Proteinase K was added to the ligation reactions and left at 65°C overnight, then the DNA was cleaned by phenol:cholorform:isoamyl alcohol extraction followed by ethanol precipitation. .. First, we digested 3 μg of each 3C library with 4 units of FatI (NEB) for 4 hours at 55 degrees.

    Spectrophotometry:

    Article Title: GENETIC DISSECTION OF INTERMALE AGGRESSIVE BEHAVIOR IN BALB/cJ AND A/J MICE
    Article Snippet: .. The concentration of the PCR product was measured using a spectrophotometer, and 2.4 μg of DNA was digested by incubating 2 units of FatI restriction enzyme and buffer (New England Biolabs, Ipswich, MA) at 55°C for 1 hour. .. The digested and undigested PCR products were electrophoresed side-by-side on a 10% polyacrylamide gel and visualized using ethidium bromide staining.

    Concentration Assay:

    Article Title: GENETIC DISSECTION OF INTERMALE AGGRESSIVE BEHAVIOR IN BALB/cJ AND A/J MICE
    Article Snippet: .. The concentration of the PCR product was measured using a spectrophotometer, and 2.4 μg of DNA was digested by incubating 2 units of FatI restriction enzyme and buffer (New England Biolabs, Ipswich, MA) at 55°C for 1 hour. .. The digested and undigested PCR products were electrophoresed side-by-side on a 10% polyacrylamide gel and visualized using ethidium bromide staining.

    BAC Assay:

    Article Title: Epigenetic Control of Cell Cycle-Dependent Histone Gene Expression Is a Principal Component of the Abbreviated Pluripotent Cell Cycle
    Article Snippet: Nuclei were digested with FatI (R0650, New England BioLabs) for 2 h at 55°C and then overnight at 42°C. .. To control for primer efficiency and to serve as a random ligation control, a bacterial artificial chromosome (BAC) (RP11-1118G19; BACPAC) spanning the histone HIST2H4 region was used.

    Article Title: ETV1 positively regulates transcription of tumor suppressor ARF
    Article Snippet: In order to construct ARF luciferase reporter (pARF-luc), a fragment of human genomic DNA was amplified from BAC clone 478M20 (acquired from a library at Roswell Park Cancer Institute) using GCCGCTCCTT CCTTTCCTTG and GATGACTCCT CGGTCGCAGA primers. .. The PCR fragment was cut FatI (New England Biolabs, R0650) and RsaI (New England Biolabs, R0167) and inserted between EcoIRCI (Promega, R6951) and NcoI (New England Biolabs, R0193) sites of pGL3 Basic immediately upstream of the Luciferase gene.

    Staining:

    Article Title: ETV1 positively regulates transcription of tumor suppressor ARF
    Article Snippet: Cell numbers were compared using methylene blue staining and extraction method. .. The PCR fragment was cut FatI (New England Biolabs, R0650) and RsaI (New England Biolabs, R0167) and inserted between EcoIRCI (Promega, R6951) and NcoI (New England Biolabs, R0193) sites of pGL3 Basic immediately upstream of the Luciferase gene.

    Article Title: GENETIC DISSECTION OF INTERMALE AGGRESSIVE BEHAVIOR IN BALB/cJ AND A/J MICE
    Article Snippet: The concentration of the PCR product was measured using a spectrophotometer, and 2.4 μg of DNA was digested by incubating 2 units of FatI restriction enzyme and buffer (New England Biolabs, Ipswich, MA) at 55°C for 1 hour. .. The digested and undigested PCR products were electrophoresed side-by-side on a 10% polyacrylamide gel and visualized using ethidium bromide staining.

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  • 88
    New England Biolabs fati restriction enzyme
    Fati Restriction Enzyme, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 88/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fati restriction enzyme/product/New England Biolabs
    Average 88 stars, based on 6 article reviews
    Price from $9.99 to $1999.99
    fati restriction enzyme - by Bioz Stars, 2020-04
    88/100 stars
      Buy from Supplier

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