polyclonal goat anti human il 15 ab Search Results


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Bio-Techne corporation human il-17/il-17a antibody
Human Il 17/Il 17a Antibody, supplied by Bio-Techne corporation, 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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ImmunoReagents inc goat polyclonal anti-human psa antibody (designated as ab 2 )
Goat Polyclonal Anti Human Psa Antibody (Designated As Ab 2 ), supplied by ImmunoReagents 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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PeproTech goat anti-human fasl polyclonal ab (peprotech inc)
Goat Anti Human Fasl Polyclonal Ab (Peprotech Inc), supplied by PeproTech, 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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Upstate Biotechnology Inc polyclonal goat anti-human pdgf-ab
Polyclonal Goat Anti Human Pdgf Ab, supplied by Upstate Biotechnology 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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Merck KGaA alkaline phosphatase-conjugated goat anti-human immunoglobulin antibody
Western blot analysis of the recombinant proteins from P. brasiliensis recognized by sera from patients with paracoccidioidomycosis (PCM) or healthy subjects (NC). Recombinant proteins were separated by SDS-PAGE and transferred to nitrocellulose membranes. Membranes containing both proteins were incubated with sera from PCM patients ( A ) or NC subjects ( B ). After incubation with <t>alkaline-phosphatase-conjugated</t> antibody to human <t>immunoglobulin,</t> the reactions were revealed with BCIP-NBT. The arrowheads indicate the migration position of rPbHsp60 and rgp43. The identification of each patient serum is depicted by the numbers below each image. The negative reaction for both proteins is not shown. C , Relative number (%) of positive reactions with serum samples from PCM patients and NC group against rPbHsp60 and rgp43. No NC serum was reactive to rgp43.
Alkaline Phosphatase Conjugated Goat Anti Human Immunoglobulin Antibody, supplied by Merck KGaA, 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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PeproTech goat polyclonal anti-human tweak ab
Western blot analysis of the recombinant proteins from P. brasiliensis recognized by sera from patients with paracoccidioidomycosis (PCM) or healthy subjects (NC). Recombinant proteins were separated by SDS-PAGE and transferred to nitrocellulose membranes. Membranes containing both proteins were incubated with sera from PCM patients ( A ) or NC subjects ( B ). After incubation with <t>alkaline-phosphatase-conjugated</t> antibody to human <t>immunoglobulin,</t> the reactions were revealed with BCIP-NBT. The arrowheads indicate the migration position of rPbHsp60 and rgp43. The identification of each patient serum is depicted by the numbers below each image. The negative reaction for both proteins is not shown. C , Relative number (%) of positive reactions with serum samples from PCM patients and NC group against rPbHsp60 and rgp43. No NC serum was reactive to rgp43.
Goat Polyclonal Anti Human Tweak Ab, supplied by PeproTech, 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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Cappel Laboratories polyclonal goat f(ab9)2 anti-human fc
Western blot analysis of the recombinant proteins from P. brasiliensis recognized by sera from patients with paracoccidioidomycosis (PCM) or healthy subjects (NC). Recombinant proteins were separated by SDS-PAGE and transferred to nitrocellulose membranes. Membranes containing both proteins were incubated with sera from PCM patients ( A ) or NC subjects ( B ). After incubation with <t>alkaline-phosphatase-conjugated</t> antibody to human <t>immunoglobulin,</t> the reactions were revealed with BCIP-NBT. The arrowheads indicate the migration position of rPbHsp60 and rgp43. The identification of each patient serum is depicted by the numbers below each image. The negative reaction for both proteins is not shown. C , Relative number (%) of positive reactions with serum samples from PCM patients and NC group against rPbHsp60 and rgp43. No NC serum was reactive to rgp43.
Polyclonal Goat F(Ab9)2 Anti Human Fc, supplied by Cappel Laboratories, 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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Immunotec inc polyclonal goat anti-mouse/human igm specific f(ab)' 2
Western blot analysis of the recombinant proteins from P. brasiliensis recognized by sera from patients with paracoccidioidomycosis (PCM) or healthy subjects (NC). Recombinant proteins were separated by SDS-PAGE and transferred to nitrocellulose membranes. Membranes containing both proteins were incubated with sera from PCM patients ( A ) or NC subjects ( B ). After incubation with <t>alkaline-phosphatase-conjugated</t> antibody to human <t>immunoglobulin,</t> the reactions were revealed with BCIP-NBT. The arrowheads indicate the migration position of rPbHsp60 and rgp43. The identification of each patient serum is depicted by the numbers below each image. The negative reaction for both proteins is not shown. C , Relative number (%) of positive reactions with serum samples from PCM patients and NC group against rPbHsp60 and rgp43. No NC serum was reactive to rgp43.
Polyclonal Goat Anti Mouse/Human Igm Specific F(Ab)' 2, supplied by Immunotec 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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Phoenix Pharmaceuticals polyclonal goat anti-human il-36g/il-1f9 ab
Western blot analysis of the recombinant proteins from P. brasiliensis recognized by sera from patients with paracoccidioidomycosis (PCM) or healthy subjects (NC). Recombinant proteins were separated by SDS-PAGE and transferred to nitrocellulose membranes. Membranes containing both proteins were incubated with sera from PCM patients ( A ) or NC subjects ( B ). After incubation with <t>alkaline-phosphatase-conjugated</t> antibody to human <t>immunoglobulin,</t> the reactions were revealed with BCIP-NBT. The arrowheads indicate the migration position of rPbHsp60 and rgp43. The identification of each patient serum is depicted by the numbers below each image. The negative reaction for both proteins is not shown. C , Relative number (%) of positive reactions with serum samples from PCM patients and NC group against rPbHsp60 and rgp43. No NC serum was reactive to rgp43.
Polyclonal Goat Anti Human Il 36g/Il 1f9 Ab, supplied by Phoenix Pharmaceuticals, 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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EuroClone polyclonal goat anti-human fh ab
FHR-1, FHR-5, FHL-1 and mini-FH bind to primary neutrophil granulocytes and monocytes. Binding of 300 nM of each protein (solid lines) to neutrophil granulocytes and monocytes in Ca 2+ and Mg 2+ containing DPBS was measured by flow cytometry. Filled histograms indicate autofluorescence, dotted lines show samples incubated without the proteins added (antibody controls). Binding of the added proteins (solid black line) was analyzed using <t>polyclonal</t> anti-FH Ab for FHR-1, FHL-1 and mini-FH detection, and monoclonal anti-FHR-5 for FHR-5 detection. A representative histogram out of three independent experiments is shown in each case.
Polyclonal Goat Anti Human Fh Ab, supplied by EuroClone, 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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Bio-Techne corporation human il-15 antibody
FHR-1, FHR-5, FHL-1 and mini-FH bind to primary neutrophil granulocytes and monocytes. Binding of 300 nM of each protein (solid lines) to neutrophil granulocytes and monocytes in Ca 2+ and Mg 2+ containing DPBS was measured by flow cytometry. Filled histograms indicate autofluorescence, dotted lines show samples incubated without the proteins added (antibody controls). Binding of the added proteins (solid black line) was analyzed using <t>polyclonal</t> anti-FH Ab for FHR-1, FHL-1 and mini-FH detection, and monoclonal anti-FHR-5 for FHR-5 detection. A representative histogram out of three independent experiments is shown in each case.
Human Il 15 Antibody, supplied by Bio-Techne corporation, 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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Bio-Techne corporation mouse cd45 antibody
FHR-1, FHR-5, FHL-1 and mini-FH bind to primary neutrophil granulocytes and monocytes. Binding of 300 nM of each protein (solid lines) to neutrophil granulocytes and monocytes in Ca 2+ and Mg 2+ containing DPBS was measured by flow cytometry. Filled histograms indicate autofluorescence, dotted lines show samples incubated without the proteins added (antibody controls). Binding of the added proteins (solid black line) was analyzed using <t>polyclonal</t> anti-FH Ab for FHR-1, FHL-1 and mini-FH detection, and monoclonal anti-FHR-5 for FHR-5 detection. A representative histogram out of three independent experiments is shown in each case.
Mouse Cd45 Antibody, supplied by Bio-Techne corporation, 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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Western blot analysis of the recombinant proteins from P. brasiliensis recognized by sera from patients with paracoccidioidomycosis (PCM) or healthy subjects (NC). Recombinant proteins were separated by SDS-PAGE and transferred to nitrocellulose membranes. Membranes containing both proteins were incubated with sera from PCM patients ( A ) or NC subjects ( B ). After incubation with alkaline-phosphatase-conjugated antibody to human immunoglobulin, the reactions were revealed with BCIP-NBT. The arrowheads indicate the migration position of rPbHsp60 and rgp43. The identification of each patient serum is depicted by the numbers below each image. The negative reaction for both proteins is not shown. C , Relative number (%) of positive reactions with serum samples from PCM patients and NC group against rPbHsp60 and rgp43. No NC serum was reactive to rgp43.

Journal: Brazilian Journal of Medical and Biological Research

Article Title: Recombinant 60-kDa heat shock protein from Paracoccidioides brasiliensis : is it a good antigen for serological diagnosis of paracoccidioidomycosis?

doi: 10.1590/1414-431X20175928

Figure Lengend Snippet: Western blot analysis of the recombinant proteins from P. brasiliensis recognized by sera from patients with paracoccidioidomycosis (PCM) or healthy subjects (NC). Recombinant proteins were separated by SDS-PAGE and transferred to nitrocellulose membranes. Membranes containing both proteins were incubated with sera from PCM patients ( A ) or NC subjects ( B ). After incubation with alkaline-phosphatase-conjugated antibody to human immunoglobulin, the reactions were revealed with BCIP-NBT. The arrowheads indicate the migration position of rPbHsp60 and rgp43. The identification of each patient serum is depicted by the numbers below each image. The negative reaction for both proteins is not shown. C , Relative number (%) of positive reactions with serum samples from PCM patients and NC group against rPbHsp60 and rgp43. No NC serum was reactive to rgp43.

Article Snippet: After 2 h, the plates were washed five times and the wells were incubated with 100 μL of alkaline phosphatase-conjugated goat anti-human immunoglobulin antibody (Merck Millipore) diluted to 1:2,000, at 37°C.

Techniques: Western Blot, Recombinant, SDS Page, Incubation, Migration

FHR-1, FHR-5, FHL-1 and mini-FH bind to primary neutrophil granulocytes and monocytes. Binding of 300 nM of each protein (solid lines) to neutrophil granulocytes and monocytes in Ca 2+ and Mg 2+ containing DPBS was measured by flow cytometry. Filled histograms indicate autofluorescence, dotted lines show samples incubated without the proteins added (antibody controls). Binding of the added proteins (solid black line) was analyzed using polyclonal anti-FH Ab for FHR-1, FHL-1 and mini-FH detection, and monoclonal anti-FHR-5 for FHR-5 detection. A representative histogram out of three independent experiments is shown in each case.

Journal: Frontiers in Immunology

Article Title: Complement Factor H Family Proteins Modulate Monocyte and Neutrophil Granulocyte Functions

doi: 10.3389/fimmu.2021.660852

Figure Lengend Snippet: FHR-1, FHR-5, FHL-1 and mini-FH bind to primary neutrophil granulocytes and monocytes. Binding of 300 nM of each protein (solid lines) to neutrophil granulocytes and monocytes in Ca 2+ and Mg 2+ containing DPBS was measured by flow cytometry. Filled histograms indicate autofluorescence, dotted lines show samples incubated without the proteins added (antibody controls). Binding of the added proteins (solid black line) was analyzed using polyclonal anti-FH Ab for FHR-1, FHL-1 and mini-FH detection, and monoclonal anti-FHR-5 for FHR-5 detection. A representative histogram out of three independent experiments is shown in each case.

Article Snippet: Bound proteins were detected via incubation with the polyclonal goat anti-human FH Ab in DPBS containing fetal bovine serum (FBS, 0.1%, EuroClone, Pero, Italy) for 15 minutes at 4°C, washed and labelled with Alexa-488-conjugated rabbit anti-goat antibody (Thermo Scientific, Waltham, MA) under the same conditions.

Techniques: Binding Assay, Flow Cytometry, Incubation