secondary polymer antibodies Search Results


91
Novus Biologicals horse anti mouse
Horse Anti Mouse, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novus Biologicals anti mouse igg secondary antibody
Anti Mouse Igg Secondary Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novus Biologicals goat antirabbit hrp lmg goat mab novus biologicals
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Novus Biologicals immpress anti rabbit igg
Immpress Anti Rabbit Igg, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems polyclonal goat anti mouse mmp 2
Polyclonal Goat Anti Mouse Mmp 2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novus Biologicals horse polyclonal anti hbs antibody
FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a <t>polyclonal</t> S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.
Horse Polyclonal Anti Hbs Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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Novus Biologicals goat anti horse hrp antibody
FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a <t>polyclonal</t> S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.
Goat Anti Horse Hrp Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biocare Medical secondary antibody hrp-polymers
FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a <t>polyclonal</t> S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.
Secondary Antibody Hrp Polymers, supplied by Biocare Medical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GeneTex onestep polymer hrp-conjugated anti-mouse/rat/rabbit igg secondary antibody gtx83398
FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a <t>polyclonal</t> S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.
Onestep Polymer Hrp Conjugated Anti Mouse/Rat/Rabbit Igg Secondary Antibody Gtx83398, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Maxim Biotech Inc horseradish peroxidase conjugated-polymer anti-mouse secondary antibody
FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a <t>polyclonal</t> S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.
Horseradish Peroxidase Conjugated Polymer Anti Mouse Secondary Antibody, supplied by Maxim Biotech Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Biogenex polymer–horseradish peroxidise (hrp) reagent
FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a <t>polyclonal</t> S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.
Polymer–Horseradish Peroxidise (Hrp) Reagent, supplied by Biogenex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biogenex secondary antibody containing super sensitive polymer dab detection kit
FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a <t>polyclonal</t> S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.
Secondary Antibody Containing Super Sensitive Polymer Dab Detection Kit, supplied by Biogenex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a polyclonal S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.

Journal: Journal of Clinical Microbiology

Article Title: Improved Method for Rapid and Efficient Determination of Genome Replication and Protein Expression of Clinical Hepatitis B Virus Isolates

doi: 10.1128/jcm.02340-10

Figure Lengend Snippet: FIG. 5. Genome replication, virion secretion, and protein expression of PCR clones derived from two thermophilic DNA polymerases. The 4B genome was amplified by 30 cycles of PCR using either High Fidelityplus DNA polymerase or Phusion DNA polymerase and then cloned. The PCR clones were digested with BspQI and further treated with T4 DNA ligase before transfection to Huh7 cells. The uncut original EcoRI dimer of clone 4B served as a positive control for transfection. (A) A fraction of the purified DNA prior to transfection, with the first lane being HindIII-digested DNA. (D) Intracellular envelope proteins were detected by a monoclonal preS2 antibody (specific for the L and M proteins) and a polyclonal S antibody from Novus (less efficient at detecting L and M proteins) or just by the S antibody.

Article Snippet: Virus particles were immunoprecipitated from culture supernatant with a horse polyclonal anti-HBs antibody (Ad/Ay; Novus).

Techniques: Expressing, Clone Assay, Derivative Assay, Transfection, Positive Control