avian myeloblastosis virus amv rtase Search Results


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  • 86
    Millipore avian myeloblastosis virus rt amv rt
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    Thermo Fisher avian myeloblastosis virus amv rtase
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    Thermo Fisher avian myeloblastosis virus rt
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
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    Boehringer Mannheim avian myeloblastosis virus rt
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
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    Roche avian myeloblastosis virus rt
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
    Avian Myeloblastosis Virus Rt, supplied by Roche, used in various techniques. Bioz Stars score: 90/100, based on 38 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega avian myeloblastosis virus amv rt enzyme
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
    Avian Myeloblastosis Virus Amv Rt Enzyme, supplied by Promega, used in various techniques. Bioz Stars score: 85/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Promega rt avian myeloblastosis virus amv buffer
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
    Rt Avian Myeloblastosis Virus Amv Buffer, supplied by Promega, used in various techniques. Bioz Stars score: 85/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Roche rt pcr avian myeloblastosis virus amv
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
    Rt Pcr Avian Myeloblastosis Virus Amv, supplied by Roche, used in various techniques. Bioz Stars score: 85/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    TaKaRa avian myeloblastosis virus reverse transcriptase
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
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    Boehringer Mannheim avian myeloblastosis virus reverse transcriptase
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
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    Promega avian myeloblastosis virus rtase
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
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    Roche avian myeloblastosis virus reverse transcriptase amv rt
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
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    Stratagene avian myeloblastosis virus rt
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
    Avian Myeloblastosis Virus Rt, supplied by Stratagene, used in various techniques. Bioz Stars score: 90/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher avian myeloblastosis virus reverse transcription
    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian <t>myeloblastosis</t> virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.
    Avian Myeloblastosis Virus Reverse Transcription, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian myeloblastosis virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.

    Journal: Journal of Virology

    Article Title: Association of Human Immunodeficiency Virus Type 1 Vif with RNA and Its Role in Reverse Transcription

    doi:

    Figure Lengend Snippet: Association of Vif with viral genomic RNA. (A) H9 cell lysates from mock-infected cells or cells expressing the wild type (wt) or vif mutant (vifΔ) were subjected to immunoprecipitation with antiserum against Vif. Immunoprecipitated pellets were either directly PCR amplified with primers directed against the HIV-1 genome, or cDNA synthesis was performed first with avian myeloblastosis virus RT, followed by PCR. Direct PCR amplification were performed on the HXB2 construct as a positive control. MW, molecular weight markers; nt, nucleotides. (B) RNA of H9 cell lysates from mock-infected cells or cells expressing the wild type or vif mutant were subjected to RNase protection with a probe to the HIV-1 genome. (C) Western blot analysis of cell lysates was performed with antiserum against Vif. (D) Amino acid sequence alignment of HIV-1 Vif and Xlrbpa. Residues in boldface display the highly conserved Vif sequence among lentiviruses. Shaded residues display sequence identity between HIV-1 Vif and Xlrbpa.

    Article Snippet: Precipitated samples were subjected to either cDNA synthesis with avian myeloblastosis virus RT (Invitrogen), followed by PCR, or were submitted directly to PCR.

    Techniques: Infection, Expressing, Mutagenesis, Immunoprecipitation, Polymerase Chain Reaction, Amplification, Construct, Positive Control, Molecular Weight, Western Blot, Sequencing