fitc anti rabbit Search Results


800cw conjugated affinity purified anti rabbit  (Rockland Immunochemicals)
93
Rockland Immunochemicals 800cw conjugated affinity purified anti rabbit
800cw Conjugated Affinity Purified Anti Rabbit, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/pmc02756010-47-10-22?v=Rockland+Immunochemicals
Average 93 stars, based on 1 article reviews
800cw conjugated affinity purified anti rabbit - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier
fitc goat anti rabbit igg  (Rockland Immunochemicals)
85
Rockland Immunochemicals fitc goat anti rabbit igg
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Fitc Goat Anti Rabbit Igg, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/pmc02936550-236-18-22?v=Rockland+Immunochemicals
Average 85 stars, based on 1 article reviews
fitc goat anti rabbit igg - by Bioz Stars, 2026-08
85/100 stars
  Buy from Supplier
rabbit polyclonal anti collagen iv  (Rockland Immunochemicals)
93
Rockland Immunochemicals rabbit polyclonal anti collagen iv
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Rabbit Polyclonal Anti Collagen Iv, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/pmc08960062-122-28-33?v=Rockland+Immunochemicals
Average 93 stars, based on 1 article reviews
rabbit polyclonal anti collagen iv - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier
fluorescein isothiocyanate conjugated polymorphonuclear leukocytes  (Cedarlane)
90
Cedarlane fluorescein isothiocyanate conjugated polymorphonuclear leukocytes
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Fluorescein Isothiocyanate Conjugated Polymorphonuclear Leukocytes, supplied by Cedarlane, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/pmc04954452-218-13-19?v=Cedarlane
Average 90 stars, based on 1 article reviews
fluorescein isothiocyanate conjugated polymorphonuclear leukocytes - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier
horseradish peroxidase  (Cedarlane)
93
Cedarlane horseradish peroxidase
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Horseradish Peroxidase, supplied by Cedarlane, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/pmc04294392-164-17-22?v=Cedarlane
Average 93 stars, based on 1 article reviews
horseradish peroxidase - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier
rabbit anti fitc hrp antibody  (Bio-Rad)
95
Bio-Rad rabbit anti fitc hrp antibody
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Rabbit Anti Fitc Hrp Antibody, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/us11859008-1416-18-21?v=Bio-Rad
Average 95 stars, based on 1 article reviews
rabbit anti fitc hrp antibody - by Bioz Stars, 2026-08
95/100 stars
  Buy from Supplier
fitc conjugated goat anti rabbit  (Jackson Immuno)
96
Jackson Immuno fitc conjugated goat anti rabbit
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Fitc Conjugated Goat Anti Rabbit, 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
https://www.bioz.com/product/fitc+anti+rabbit/bio_rxiv__64898__2026__01__28__702397-278-4-7?v=Jackson+Immuno
Average 96 stars, based on 1 article reviews
fitc conjugated goat anti rabbit - by Bioz Stars, 2026-08
96/100 stars
  Buy from Supplier
anti mouse antibody  (Jackson Immuno)
85
Jackson Immuno anti mouse antibody
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Anti Mouse Antibody, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/pm41688418-385-6-16?v=Jackson+Immuno
Average 85 stars, based on 1 article reviews
anti mouse antibody - by Bioz Stars, 2026-08
85/100 stars
  Buy from Supplier
pbs  (Jackson Immuno)
93
Jackson Immuno pbs
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Pbs, 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
https://www.bioz.com/product/fitc+anti+rabbit/pmc04541502-99-10-24?v=Jackson+Immuno
Average 93 stars, based on 1 article reviews
pbs - by Bioz Stars, 2026-08
93/100 stars
  Buy from Supplier
anti rabbit igg  (Jackson Immuno)
96
Jackson Immuno anti rabbit igg
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Anti Rabbit Igg, 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
https://www.bioz.com/product/fitc+anti+rabbit/pm18239674-165-51-56?v=Jackson+Immuno
Average 96 stars, based on 1 article reviews
anti rabbit igg - by Bioz Stars, 2026-08
96/100 stars
  Buy from Supplier
hamster igg  (Jackson Immuno)
94
Jackson Immuno hamster igg
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Hamster 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
https://www.bioz.com/product/fitc+anti+rabbit/pm12080475-190-3-10?v=Jackson+Immuno
Average 94 stars, based on 1 article reviews
hamster igg - by Bioz Stars, 2026-08
94/100 stars
  Buy from Supplier
anti rabbit igg antibodies  (Santa Cruz Biotechnology)
94
Santa Cruz Biotechnology anti rabbit igg antibodies
(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by <t>FITC-labeled</t> secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).
Anti Rabbit Igg Antibodies, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+anti+rabbit/pmc02265955-181-1-7?v=Santa+Cruz+Biotechnology
Average 94 stars, based on 1 article reviews
anti rabbit igg antibodies - by Bioz Stars, 2026-08
94/100 stars
  Buy from Supplier

Image Search Results


(A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by FITC-labeled secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).

Journal: PLoS Pathogens

Article Title: Steric Shielding of Surface Epitopes and Impaired Immune Recognition Induced by the Ebola Virus Glycoprotein

doi: 10.1371/journal.ppat.1001098

Figure Lengend Snippet: (A) 293T cells were transfected with empty pCAGGS (vector) or vector encoding GP. Floating and adherent cells were harvested 24 h after transfection, pooled, and stained for GP using the KZ52 antibody, followed by FITC-labeled secondary antibodies, and co-stained for β1 integrin or MHC1 with PE-Cy5 conjugated monoclonal antibodies and assayed by flow cytometry. (B) Following transfection with vector encoding GP, floating 293T cells were removed from adherent cells, stained for β1 integrin and assayed by flow cytometry (left panel). Similarly treated cells were mounted on coverslips, fixed, permeabilized and stained for GP with mouse monoclonal antibodies, followed by Alexa 594 conjugated antibodies and assayed by immunofluorescence microscopy. A representative cell is shown (right panel).

Article Snippet: For detection of AU1 epitopes, cells were stained with rabbit polyclonal anti-AU1 antibodies (Bethyl labs) and detected with FITC goat anti-rabbit IgG (Rockland).

Techniques: Transfection, Plasmid Preparation, Staining, Labeling, Bioprocessing, Flow Cytometry, Immunofluorescence, Microscopy

OV79 SL9 target cells were mock transduced (no Ad) or transduced with Adenoviral vectors expressing GFP (Ad GFP) or GFP and EBOV GP (Ad GP) at an MOI of 300. 48 h after transduction, cells were assayed for GFP expression (A); No Ad = blue trace; Ad GFP = green trace; Ad GP = orange trace. Cells were also stained for MHC1 (B); isotype antibody = shaded peak; No Ad = blue trace; Ad GFP = green trace; Ad GP = orange trace. In parallel, CD8 T cells expressing a transgenic TCR (868TCRwt) that recognizes the SL9 HLA-A2 complex were incubated alone or with mock- (no Ad) or Ad- transduced target cells in a 2∶1 ratio. After co-culture, T cells were surface stained for CD8, then fixed and permeabilized, and stained for 868TCRwt and MIP-1β with APC-H7, FITC, and PE- conjugated antibodies, respectively, and assayed by flow cytometry. (C) CD8 + and 868TCRwt + events were analyzed for MIP-1β staining. (D) Bar graph depicts percent cells positive for MIP-1β, normalized to the No Ad target cell sample.

Journal: PLoS Pathogens

Article Title: Steric Shielding of Surface Epitopes and Impaired Immune Recognition Induced by the Ebola Virus Glycoprotein

doi: 10.1371/journal.ppat.1001098

Figure Lengend Snippet: OV79 SL9 target cells were mock transduced (no Ad) or transduced with Adenoviral vectors expressing GFP (Ad GFP) or GFP and EBOV GP (Ad GP) at an MOI of 300. 48 h after transduction, cells were assayed for GFP expression (A); No Ad = blue trace; Ad GFP = green trace; Ad GP = orange trace. Cells were also stained for MHC1 (B); isotype antibody = shaded peak; No Ad = blue trace; Ad GFP = green trace; Ad GP = orange trace. In parallel, CD8 T cells expressing a transgenic TCR (868TCRwt) that recognizes the SL9 HLA-A2 complex were incubated alone or with mock- (no Ad) or Ad- transduced target cells in a 2∶1 ratio. After co-culture, T cells were surface stained for CD8, then fixed and permeabilized, and stained for 868TCRwt and MIP-1β with APC-H7, FITC, and PE- conjugated antibodies, respectively, and assayed by flow cytometry. (C) CD8 + and 868TCRwt + events were analyzed for MIP-1β staining. (D) Bar graph depicts percent cells positive for MIP-1β, normalized to the No Ad target cell sample.

Article Snippet: For detection of AU1 epitopes, cells were stained with rabbit polyclonal anti-AU1 antibodies (Bethyl labs) and detected with FITC goat anti-rabbit IgG (Rockland).

Techniques: Transduction, Expressing, Staining, Transgenic Assay, Incubation, Co-Culture Assay, Flow Cytometry