genomic dna contamination  (TaKaRa)


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    TaKaRa genomic dna contamination
    Genomic Dna Contamination, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    genomic dna contamination - by Bioz Stars, 2024-09
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    genomic dna contamination  (TaKaRa)


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    TaKaRa genomic dna contamination
    Genomic Dna Contamination, supplied by TaKaRa, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/genomic dna contamination/product/TaKaRa
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    genomic dna contamination  (Thermo Fisher)


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    Thermo Fisher genomic dna contamination
    Genomic Dna Contamination, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/genomic dna contamination/product/Thermo Fisher
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    Aidlab Inc genomic dna contamination
    Genomic Dna Contamination, supplied by Aidlab Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/genomic dna contamination/product/Aidlab Inc
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    genomic dna contamination  (MedChemExpress)


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    MedChemExpress genomic dna contamination
    MGF_360-4L is a critical virulence gene of ASFV. (A) Rectal temperatures of pigs were measured daily after intramuscular injection of ASFV-WT (20 HAD 50 ) or ASFV-ΔMGF_360-4L (20 HAD 50 , 100 HAD 50 ) (n=5). (B) Survival rates of pigs were calculated. (C-D) qPCR analysis of ASFV <t>genomic</t> <t>DNA</t> copy number in blood, oral, nasal, and anal swabs obtained from pigs after infection with either ASFV-ΔMGF_360-4L or ASFV-WT. (E) qPCR analysis of ASFV genomic DNA copy number in various organs (heart, liver, spleen, lung, kidney, submandibular lymph nodes, mesenteric lymph nodes, inguinal lymph nodes, and tonsils) from pigs infected with ASFV-ΔMGF_360-4L or ASFV-WT.
    Genomic Dna Contamination, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/genomic dna contamination/product/MedChemExpress
    Average 86 stars, based on 1 article reviews
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    genomic dna contamination - by Bioz Stars, 2024-09
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    1) Product Images from "The African Swine Fever Virus gene MGF_360-4L inhibits interferon signaling by recruiting mitochondrial selective autophagy receptor SQSTM1 degrading MDA5 antagonizing innate immune responses"

    Article Title: The African Swine Fever Virus gene MGF_360-4L inhibits interferon signaling by recruiting mitochondrial selective autophagy receptor SQSTM1 degrading MDA5 antagonizing innate immune responses

    Journal: bioRxiv

    doi: 10.1101/2024.09.09.612163

    MGF_360-4L is a critical virulence gene of ASFV. (A) Rectal temperatures of pigs were measured daily after intramuscular injection of ASFV-WT (20 HAD 50 ) or ASFV-ΔMGF_360-4L (20 HAD 50 , 100 HAD 50 ) (n=5). (B) Survival rates of pigs were calculated. (C-D) qPCR analysis of ASFV genomic DNA copy number in blood, oral, nasal, and anal swabs obtained from pigs after infection with either ASFV-ΔMGF_360-4L or ASFV-WT. (E) qPCR analysis of ASFV genomic DNA copy number in various organs (heart, liver, spleen, lung, kidney, submandibular lymph nodes, mesenteric lymph nodes, inguinal lymph nodes, and tonsils) from pigs infected with ASFV-ΔMGF_360-4L or ASFV-WT.
    Figure Legend Snippet: MGF_360-4L is a critical virulence gene of ASFV. (A) Rectal temperatures of pigs were measured daily after intramuscular injection of ASFV-WT (20 HAD 50 ) or ASFV-ΔMGF_360-4L (20 HAD 50 , 100 HAD 50 ) (n=5). (B) Survival rates of pigs were calculated. (C-D) qPCR analysis of ASFV genomic DNA copy number in blood, oral, nasal, and anal swabs obtained from pigs after infection with either ASFV-ΔMGF_360-4L or ASFV-WT. (E) qPCR analysis of ASFV genomic DNA copy number in various organs (heart, liver, spleen, lung, kidney, submandibular lymph nodes, mesenteric lymph nodes, inguinal lymph nodes, and tonsils) from pigs infected with ASFV-ΔMGF_360-4L or ASFV-WT.

    Techniques Used: Injection, Infection

    genomic dna contamination  (New England Biolabs)


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    New England Biolabs genomic dna contamination
    Genomic Dna Contamination, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/genomic dna contamination/product/New England Biolabs
    Average 86 stars, based on 1 article reviews
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    genomic dna contamination  (Thermo Fisher)


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    Thermo Fisher genomic dna contamination
    (A) Quantitative PCR (qPCR) analyses of the spatial expression profile of HYC2 in various tissues of 7-day-old seedlings (Se), roots (Ro), rosette leaves (RL), cauline leaves (CL), shoots (Sh), buds (bu), flowers (Fl), and siliques (Si), as well as genomic <t>DNA</t> <t>(gDNA).</t> ACT1 was the internal control for normalization. The primer pairs for the internal control gene ACT1 were designed to span introns, confirming the absence of genomic DNA contamination in all cDNA samples. The number on the right side indicates the number of amplification cycles for PCR. (B) Schematic representation of HYC2 protein variants in the complementation assay. The number of amino acids is specified, and the black region signifies the Hyccin domain.
    Genomic Dna Contamination, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Recruitment of SH3P2–DRP1A by HYCCIN2 Drives Membrane Tubulation in Arabidopsis Embryonic Cell Plate Formation"

    Article Title: Recruitment of SH3P2–DRP1A by HYCCIN2 Drives Membrane Tubulation in Arabidopsis Embryonic Cell Plate Formation

    Journal: bioRxiv

    doi: 10.1101/2024.09.06.611148

    (A) Quantitative PCR (qPCR) analyses of the spatial expression profile of HYC2 in various tissues of 7-day-old seedlings (Se), roots (Ro), rosette leaves (RL), cauline leaves (CL), shoots (Sh), buds (bu), flowers (Fl), and siliques (Si), as well as genomic DNA (gDNA). ACT1 was the internal control for normalization. The primer pairs for the internal control gene ACT1 were designed to span introns, confirming the absence of genomic DNA contamination in all cDNA samples. The number on the right side indicates the number of amplification cycles for PCR. (B) Schematic representation of HYC2 protein variants in the complementation assay. The number of amino acids is specified, and the black region signifies the Hyccin domain.
    Figure Legend Snippet: (A) Quantitative PCR (qPCR) analyses of the spatial expression profile of HYC2 in various tissues of 7-day-old seedlings (Se), roots (Ro), rosette leaves (RL), cauline leaves (CL), shoots (Sh), buds (bu), flowers (Fl), and siliques (Si), as well as genomic DNA (gDNA). ACT1 was the internal control for normalization. The primer pairs for the internal control gene ACT1 were designed to span introns, confirming the absence of genomic DNA contamination in all cDNA samples. The number on the right side indicates the number of amplification cycles for PCR. (B) Schematic representation of HYC2 protein variants in the complementation assay. The number of amino acids is specified, and the black region signifies the Hyccin domain.

    Techniques Used: Real-time Polymerase Chain Reaction, Expressing, Control, Amplification

    potential genomic dna contaminations  (Thermo Fisher)


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    Thermo Fisher potential genomic dna contaminations
    (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic <t>DNA</t> <t>(gDNA)</t> PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.
    Potential Genomic Dna Contaminations, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Knocking out the carboxyltransferase interactor 1 (CTI1) in Chlamydomonas boosted oil content by fivefold without affecting cell growth"

    Article Title: Knocking out the carboxyltransferase interactor 1 (CTI1) in Chlamydomonas boosted oil content by fivefold without affecting cell growth

    Journal: bioRxiv

    doi: 10.1101/2024.09.03.611075

    (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic DNA (gDNA) PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.
    Figure Legend Snippet: (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic DNA (gDNA) PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.

    Techniques Used: Sequencing, Reverse Transcription Polymerase Chain Reaction, Expressing, Marker


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    tiangen biotech co genomic dna contamination
    Genomic Dna Contamination, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Lucigen Corp genomic dna contamination
    Genomic Dna Contamination, supplied by Lucigen Corp, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 86 stars, based on 1 article reviews
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    TaKaRa genomic dna contamination
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    MGF_360-4L is a critical virulence gene of ASFV. (A) Rectal temperatures of pigs were measured daily after intramuscular injection of ASFV-WT (20 HAD 50 ) or ASFV-ΔMGF_360-4L (20 HAD 50 , 100 HAD 50 ) (n=5). (B) Survival rates of pigs were calculated. (C-D) qPCR analysis of ASFV <t>genomic</t> <t>DNA</t> copy number in blood, oral, nasal, and anal swabs obtained from pigs after infection with either ASFV-ΔMGF_360-4L or ASFV-WT. (E) qPCR analysis of ASFV genomic DNA copy number in various organs (heart, liver, spleen, lung, kidney, submandibular lymph nodes, mesenteric lymph nodes, inguinal lymph nodes, and tonsils) from pigs infected with ASFV-ΔMGF_360-4L or ASFV-WT.
    Genomic Dna Contamination, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    New England Biolabs genomic dna contamination
    MGF_360-4L is a critical virulence gene of ASFV. (A) Rectal temperatures of pigs were measured daily after intramuscular injection of ASFV-WT (20 HAD 50 ) or ASFV-ΔMGF_360-4L (20 HAD 50 , 100 HAD 50 ) (n=5). (B) Survival rates of pigs were calculated. (C-D) qPCR analysis of ASFV <t>genomic</t> <t>DNA</t> copy number in blood, oral, nasal, and anal swabs obtained from pigs after infection with either ASFV-ΔMGF_360-4L or ASFV-WT. (E) qPCR analysis of ASFV genomic DNA copy number in various organs (heart, liver, spleen, lung, kidney, submandibular lymph nodes, mesenteric lymph nodes, inguinal lymph nodes, and tonsils) from pigs infected with ASFV-ΔMGF_360-4L or ASFV-WT.
    Genomic Dna Contamination, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher potential genomic dna contaminations
    (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic <t>DNA</t> <t>(gDNA)</t> PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.
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    tiangen biotech co genomic dna contamination
    (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic <t>DNA</t> <t>(gDNA)</t> PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.
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    (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic <t>DNA</t> <t>(gDNA)</t> PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.
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    MGF_360-4L is a critical virulence gene of ASFV. (A) Rectal temperatures of pigs were measured daily after intramuscular injection of ASFV-WT (20 HAD 50 ) or ASFV-ΔMGF_360-4L (20 HAD 50 , 100 HAD 50 ) (n=5). (B) Survival rates of pigs were calculated. (C-D) qPCR analysis of ASFV genomic DNA copy number in blood, oral, nasal, and anal swabs obtained from pigs after infection with either ASFV-ΔMGF_360-4L or ASFV-WT. (E) qPCR analysis of ASFV genomic DNA copy number in various organs (heart, liver, spleen, lung, kidney, submandibular lymph nodes, mesenteric lymph nodes, inguinal lymph nodes, and tonsils) from pigs infected with ASFV-ΔMGF_360-4L or ASFV-WT.

    Journal: bioRxiv

    Article Title: The African Swine Fever Virus gene MGF_360-4L inhibits interferon signaling by recruiting mitochondrial selective autophagy receptor SQSTM1 degrading MDA5 antagonizing innate immune responses

    doi: 10.1101/2024.09.09.612163

    Figure Lengend Snippet: MGF_360-4L is a critical virulence gene of ASFV. (A) Rectal temperatures of pigs were measured daily after intramuscular injection of ASFV-WT (20 HAD 50 ) or ASFV-ΔMGF_360-4L (20 HAD 50 , 100 HAD 50 ) (n=5). (B) Survival rates of pigs were calculated. (C-D) qPCR analysis of ASFV genomic DNA copy number in blood, oral, nasal, and anal swabs obtained from pigs after infection with either ASFV-ΔMGF_360-4L or ASFV-WT. (E) qPCR analysis of ASFV genomic DNA copy number in various organs (heart, liver, spleen, lung, kidney, submandibular lymph nodes, mesenteric lymph nodes, inguinal lymph nodes, and tonsils) from pigs infected with ASFV-ΔMGF_360-4L or ASFV-WT.

    Article Snippet: Then, genomic DNA contamination was removed from the RNA template using a gDNA digester (MCE, HY-K0511A) following the manufacturer’s protocol, and reverse transcription was performed to obtain cDNA.

    Techniques: Injection, Infection

    (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic DNA (gDNA) PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.

    Journal: bioRxiv

    Article Title: Knocking out the carboxyltransferase interactor 1 (CTI1) in Chlamydomonas boosted oil content by fivefold without affecting cell growth

    doi: 10.1101/2024.09.03.611075

    Figure Lengend Snippet: (A) The sgRNA target site on CrCTI1 gene. Black arrow boxes with number stand for exons, and the black line represent the introns. (B) Genomic DNA (gDNA) PCR verification of cassette insertion in the crcti1 mutants. (C) Sanger sequencing results. (D) RT-PCR analyses of CrCTI1 expression in WT and the three crcti1 mutants. RACK1 , receptor for activated kinase C 1 was used as reference gene. M, marker; WT, wild type; PAM: protospacer adjacent motif.

    Article Snippet: To remove potential genomic DNA contaminations, the total RNA extracts were incubated with TURBO TM DNase (Life technologies).

    Techniques: Sequencing, Reverse Transcription Polymerase Chain Reaction, Expressing, Marker