Chicken Search Results


anti chicken igg  (Bioss)
90
Bioss anti chicken igg
Generation and coinfection of rTS-H9 and rTS-gB in vitro . (A) Schematic diagram depicting the rNDV cDNA clones rTS-H9 and rTS-gB. (B, C) Viral growth kinetics in BHK-21 (B) and CEF (C) cells. The cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.01. Viral titers in culture supernatants collected at 12-hour intervals were determined by IFA on the indicated cell lines. For rTS-H9 + rTS-gB: the proliferation of rTS-H9 was detected using an anti-HA primary antibody. For rTS-gB + rTS-H9: the proliferation of rTS-gB was assessed via an anti-gB primary antibody. (D, E) Foreign protein expression analysis by IFA in BHK-21 (D) and CEF (E) cells. The cells were coinfected or individually infected with rTS-H9 and/or the rTS-gB mixture at an MOI of 0.01. At 48 hpi, the cells were fixed and stained with chicken anti-HA (H9N2) and rabbit anti-gB (ILTV) antibodies, followed <t>by</t> <t>anti-chicken</t> IgG (FITC, green) and rabbit anti-IgG (Cy3, red) antibodies. The nuclei were counterstained with DAPI (blue). Scale bar = 20 μm. (F, G) BHK-21 or CEF cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.1. Western blot analysis of BHK-21 (F) and CEF (G) cell lysates harvested at 48 hpi. Proteins were detected using specific antibodies against HA (H9N2 AIV), gB (ILTV), and NDV nucleoprotein (NP). The mouse anti-actin polyclonal antibody served as a loading control.
Anti Chicken Igg, supplied by Bioss, 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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Average 90 stars, based on 1 article reviews
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recombinant chicken  (R&D Systems)
92
R&D Systems recombinant chicken
Generation and coinfection of rTS-H9 and rTS-gB in vitro . (A) Schematic diagram depicting the rNDV cDNA clones rTS-H9 and rTS-gB. (B, C) Viral growth kinetics in BHK-21 (B) and CEF (C) cells. The cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.01. Viral titers in culture supernatants collected at 12-hour intervals were determined by IFA on the indicated cell lines. For rTS-H9 + rTS-gB: the proliferation of rTS-H9 was detected using an anti-HA primary antibody. For rTS-gB + rTS-H9: the proliferation of rTS-gB was assessed via an anti-gB primary antibody. (D, E) Foreign protein expression analysis by IFA in BHK-21 (D) and CEF (E) cells. The cells were coinfected or individually infected with rTS-H9 and/or the rTS-gB mixture at an MOI of 0.01. At 48 hpi, the cells were fixed and stained with chicken anti-HA (H9N2) and rabbit anti-gB (ILTV) antibodies, followed <t>by</t> <t>anti-chicken</t> IgG (FITC, green) and rabbit anti-IgG (Cy3, red) antibodies. The nuclei were counterstained with DAPI (blue). Scale bar = 20 μm. (F, G) BHK-21 or CEF cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.1. Western blot analysis of BHK-21 (F) and CEF (G) cell lysates harvested at 48 hpi. Proteins were detected using specific antibodies against HA (H9N2 AIV), gB (ILTV), and NDV nucleoprotein (NP). The mouse anti-actin polyclonal antibody served as a loading control.
Recombinant Chicken, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/recombinant chicken/product/R&D Systems
Average 92 stars, based on 1 article reviews
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92/100 stars
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myostatin positive sc mstn pax7  (R&D Systems)
99
R&D Systems myostatin positive sc mstn pax7
Generation and coinfection of rTS-H9 and rTS-gB in vitro . (A) Schematic diagram depicting the rNDV cDNA clones rTS-H9 and rTS-gB. (B, C) Viral growth kinetics in BHK-21 (B) and CEF (C) cells. The cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.01. Viral titers in culture supernatants collected at 12-hour intervals were determined by IFA on the indicated cell lines. For rTS-H9 + rTS-gB: the proliferation of rTS-H9 was detected using an anti-HA primary antibody. For rTS-gB + rTS-H9: the proliferation of rTS-gB was assessed via an anti-gB primary antibody. (D, E) Foreign protein expression analysis by IFA in BHK-21 (D) and CEF (E) cells. The cells were coinfected or individually infected with rTS-H9 and/or the rTS-gB mixture at an MOI of 0.01. At 48 hpi, the cells were fixed and stained with chicken anti-HA (H9N2) and rabbit anti-gB (ILTV) antibodies, followed <t>by</t> <t>anti-chicken</t> IgG (FITC, green) and rabbit anti-IgG (Cy3, red) antibodies. The nuclei were counterstained with DAPI (blue). Scale bar = 20 μm. (F, G) BHK-21 or CEF cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.1. Western blot analysis of BHK-21 (F) and CEF (G) cell lysates harvested at 48 hpi. Proteins were detected using specific antibodies against HA (H9N2 AIV), gB (ILTV), and NDV nucleoprotein (NP). The mouse anti-actin polyclonal antibody served as a loading control.
Myostatin Positive Sc Mstn Pax7, supplied by R&D Systems, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
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goat anti chicken igg  (Novus Biologicals)
92
Novus Biologicals goat anti chicken igg
Generation and coinfection of rTS-H9 and rTS-gB in vitro . (A) Schematic diagram depicting the rNDV cDNA clones rTS-H9 and rTS-gB. (B, C) Viral growth kinetics in BHK-21 (B) and CEF (C) cells. The cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.01. Viral titers in culture supernatants collected at 12-hour intervals were determined by IFA on the indicated cell lines. For rTS-H9 + rTS-gB: the proliferation of rTS-H9 was detected using an anti-HA primary antibody. For rTS-gB + rTS-H9: the proliferation of rTS-gB was assessed via an anti-gB primary antibody. (D, E) Foreign protein expression analysis by IFA in BHK-21 (D) and CEF (E) cells. The cells were coinfected or individually infected with rTS-H9 and/or the rTS-gB mixture at an MOI of 0.01. At 48 hpi, the cells were fixed and stained with chicken anti-HA (H9N2) and rabbit anti-gB (ILTV) antibodies, followed <t>by</t> <t>anti-chicken</t> IgG (FITC, green) and rabbit anti-IgG (Cy3, red) antibodies. The nuclei were counterstained with DAPI (blue). Scale bar = 20 μm. (F, G) BHK-21 or CEF cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.1. Western blot analysis of BHK-21 (F) and CEF (G) cell lysates harvested at 48 hpi. Proteins were detected using specific antibodies against HA (H9N2 AIV), gB (ILTV), and NDV nucleoprotein (NP). The mouse anti-actin polyclonal antibody served as a loading control.
Goat Anti Chicken Igg, 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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Average 92 stars, based on 1 article reviews
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o4 mab 1326 r d systems  (R&D Systems)
99
R&D Systems o4 mab 1326 r d systems
KEY RESOURCES TABLE
O4 Mab 1326 R D Systems, supplied by R&D Systems, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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igy isotype control  (R&D Systems)
92
R&D Systems igy isotype control
KEY RESOURCES TABLE
Igy Isotype Control, supplied by R&D Systems, 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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Average 92 stars, based on 1 article reviews
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antigen antibody complexes  (Bio-Rad)
96
Bio-Rad antigen antibody complexes
KEY RESOURCES TABLE
Antigen Antibody Complexes, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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polyclonal dylight 405 affinipure goat anti chicken igy igg  (Jackson Immuno)
94
Jackson Immuno polyclonal dylight 405 affinipure goat anti chicken igy igg
KEY RESOURCES TABLE
Polyclonal Dylight 405 Affinipure Goat Anti Chicken Igy Igg, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti chicken 647 jackson immunoresearch 703 605 155 ab 2340379 donkey  (Jackson Immuno)
96
Jackson Immuno anti chicken 647 jackson immunoresearch 703 605 155 ab 2340379 donkey
KEY RESOURCES TABLE
Anti Chicken 647 Jackson Immunoresearch 703 605 155 Ab 2340379 Donkey, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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chicken serum  (Jackson Immuno)
90
Jackson Immuno chicken serum
KEY RESOURCES TABLE
Chicken Serum, supplied by Jackson Immuno, 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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aminomethylcoumarin acetate conjugated donkey anti chicken igy  (Jackson Immuno)
93
Jackson Immuno aminomethylcoumarin acetate conjugated donkey anti chicken igy
KEY RESOURCES TABLE
Aminomethylcoumarin Acetate Conjugated Donkey Anti Chicken Igy, supplied by Jackson Immuno, 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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anti chicken alexa 488  (Jackson Immuno)
95
Jackson Immuno anti chicken alexa 488
KEY RESOURCES TABLE
Anti Chicken Alexa 488, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Generation and coinfection of rTS-H9 and rTS-gB in vitro . (A) Schematic diagram depicting the rNDV cDNA clones rTS-H9 and rTS-gB. (B, C) Viral growth kinetics in BHK-21 (B) and CEF (C) cells. The cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.01. Viral titers in culture supernatants collected at 12-hour intervals were determined by IFA on the indicated cell lines. For rTS-H9 + rTS-gB: the proliferation of rTS-H9 was detected using an anti-HA primary antibody. For rTS-gB + rTS-H9: the proliferation of rTS-gB was assessed via an anti-gB primary antibody. (D, E) Foreign protein expression analysis by IFA in BHK-21 (D) and CEF (E) cells. The cells were coinfected or individually infected with rTS-H9 and/or the rTS-gB mixture at an MOI of 0.01. At 48 hpi, the cells were fixed and stained with chicken anti-HA (H9N2) and rabbit anti-gB (ILTV) antibodies, followed by anti-chicken IgG (FITC, green) and rabbit anti-IgG (Cy3, red) antibodies. The nuclei were counterstained with DAPI (blue). Scale bar = 20 μm. (F, G) BHK-21 or CEF cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.1. Western blot analysis of BHK-21 (F) and CEF (G) cell lysates harvested at 48 hpi. Proteins were detected using specific antibodies against HA (H9N2 AIV), gB (ILTV), and NDV nucleoprotein (NP). The mouse anti-actin polyclonal antibody served as a loading control.

Journal: Poultry Science

Article Title: Co-immunization with two recombinant Newcastle disease viruses expressing ILTV gB and H9N2 AIV HA confers protective efficacy against three avian pathogens

doi: 10.1016/j.psj.2026.106661

Figure Lengend Snippet: Generation and coinfection of rTS-H9 and rTS-gB in vitro . (A) Schematic diagram depicting the rNDV cDNA clones rTS-H9 and rTS-gB. (B, C) Viral growth kinetics in BHK-21 (B) and CEF (C) cells. The cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.01. Viral titers in culture supernatants collected at 12-hour intervals were determined by IFA on the indicated cell lines. For rTS-H9 + rTS-gB: the proliferation of rTS-H9 was detected using an anti-HA primary antibody. For rTS-gB + rTS-H9: the proliferation of rTS-gB was assessed via an anti-gB primary antibody. (D, E) Foreign protein expression analysis by IFA in BHK-21 (D) and CEF (E) cells. The cells were coinfected or individually infected with rTS-H9 and/or the rTS-gB mixture at an MOI of 0.01. At 48 hpi, the cells were fixed and stained with chicken anti-HA (H9N2) and rabbit anti-gB (ILTV) antibodies, followed by anti-chicken IgG (FITC, green) and rabbit anti-IgG (Cy3, red) antibodies. The nuclei were counterstained with DAPI (blue). Scale bar = 20 μm. (F, G) BHK-21 or CEF cells were coinfected or individually infected with rTS-H9/rTS-gB at an MOI of 0.1. Western blot analysis of BHK-21 (F) and CEF (G) cell lysates harvested at 48 hpi. Proteins were detected using specific antibodies against HA (H9N2 AIV), gB (ILTV), and NDV nucleoprotein (NP). The mouse anti-actin polyclonal antibody served as a loading control.

Article Snippet: Subsequently, fluorescein isothiocyanate (FITC)-conjugated anti-chicken IgG (1:200. bs0310R-FITC, Bioss) and Cy3-labeled anti-rabbit IgG (1:500.

Techniques: In Vitro, Clone Assay, Infection, Expressing, Staining, Western Blot, Control

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: Variation of Human Neural Stem Cells Generating Organizer States In Vitro before Committing to Cortical Excitatory or Inhibitory Neuronal Fates

doi: 10.1016/j.celrep.2020.107599

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: The following primary antibodies were used at the concentration indicated by manufacturer’s protocol: CaM Kinase II alpha (6G9) (NB100–1983), LMX1A (NBP1–81303) Novusbio; SYNAPSIN (106 001), HOMER (160 003) Synaptic System; EGFR (Ab231), FGFR1 phosphoY654 (Ab59194), TBR1 (Ab31940), REELIN (Ab18570), CYCLIN D1 (Ab10540), FGFR2 (Ab10648), BMPR1A (Ab38560) Abcam; HES1 (11988), p-SMAD1/5 (9516), CYCLIN D1 (2926), pERK1/2 (4370), FGFR1 (9740) Cell Signaling Technology; PAX6 (PRB-278P) BioLegend; NESTIN (MAB1259), OTX2 (AF1979), PDGFR alpha (AF1062; AF307), SOX2 (AF2018; MAB2018), SOX21 (AF3538), TuJ1 (MAB1195), EGFR (AF1280), O4 (MAB 1326) R&D Systems; GFAP (Z 0334) DAKO; HES5 (sc-13859), CUX1 (sc-13024), TLE4 (sc-9125), FGFR3 (sc-9007), LHX2 (sc-19344) Santa Cruz Biotechnology; FOXP2 (ABE73), TBR1 (AB2261), REELIN (MAB5366) Millipore; FOXG1 (M227) Takara/Clontech; anti GAD65/67 was kindly gifted by Dr. Christian Geis, Hans Berger Department of Neurology, Jena University Hospital, Germany ( ).

Techniques: Virus, Plasmid Preparation, Recombinant, Transfection, Antibody Labeling, In Vitro, Microarray, Gene Expression, Derivative Assay, Software