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goat anti rabbit biotinylated secondary antibody  (Jackson Immuno)


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    Jackson Immuno goat anti rabbit biotinylated secondary antibody
    Goat Anti Rabbit Biotinylated Secondary Antibody, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 93/100, based on 34 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fc+fragment/Biotin-SP+(long+spacer)+AffiniPure+F(ab')%E2%82%82+Fragment+Goat+Anti-Rabbit+IgG%2C+Fc+fragment+specific/pmc12996694-111-14-22
    Average 93 stars, based on 34 article reviews
    goat anti rabbit biotinylated secondary antibody - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Binding Assay:

    Article Title: Deep learning-enabled scaffolding of spatial arrays of PfCSP epitopes
    Article Snippet: KDs were measured using n-Curve KinExA Analysis method provided in KinExA Pro software and described in Technology Note 229. .. To perform KinExA equilibrium experiments, the following materials were prepared: Constant Binding Partner (CBP), human IgG or Fab, was produced in Schief Lab; antigen was expressed and purified in Schief Lab; labeling antibody for IgG was Alexa Fluor 647 conjugated AffiniPure Goat Anti-HumanIgG, Fc Fragment Specific, Jackson ImmunoResearch code 109-605-008, 500 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at −80C); for Fab the labeling antibody was Alexa Fluor 647 conjugated AffiniPure Fab Fragment Goat Anti-Human IgG (H+L), Jackson ImmunoResearch code 109-607-003, 1000 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at - 20C); running buffer was the same as sample buffer and it was 1x HBS-EP+ pH 7.4 (20x stock from Teknova, Cat. No H8022) supplemented with BSA from Sigma (cat. A3294) at 1mg/ml; beads were Thermo Scientific UltraLink azlactone-activated, beaded-polyacrylamide resin cat. number 53110 and antigen was used as a cross-linked capturing reagent; and the instrument was KinExA 3200 with Autosampler model SAPIDYNE-AIM3300 (Sapidyne Instruments). ..

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: Adalimumab, a humanized IgG1 monoclonal antibody is currently used to treat inflammatory diseases.. However, a sensitive, in-house ELISA for evaluating interand intra-individual pharmacokinetic variability of adalimumab remains limited.. In this study, an ELISA was developed to measure adalimumab levels, using recombinant human TNF-α (rhTNF-α) as capture antibody.

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: .. Nde-I and BamH-I (New England Biolabs Inc., UK), adalimumab (Humira®, AbbVie, USA), microtiter costar high binding 96-well assay plates (Corning Inc., USA), skimmed milk, tryptone type-II, 3-[(3-Cholamidopropyl) dimethylammonio]-1-propane sulfonate, LB Media and Tris-Cl (Hi-Media Laboratories, India), Tween-20, IPTG, human serum matrix (Sigma Aldrich, USA), kanamycin (Calbiochem, USA), peroxidase-conjugated goat anti-human IgG specific for Fc fragment (Jackson ImmunoResearch Cat# 109-035-008), 1X phosphate-buffered saline (1X PBS), and tetramethyl benzidine (20X TMB) (Denovo Biolabs, India), Ni-NTA column in AKTA (GE-AKTASTART, Cytiva, Sweden), surface plasma resonance (SPR) and 1-ethyl-3-(3-dimethylaminopropyl) (N-hydroxy succinimide) carbodiimide in combination with N-hydroxy succinimide (EDC-NHS) (Affinite, Canada), were procured for the study. .. The rhTNF-α used as coating reagent in ELISA was commercially cloned using pET28 a (+) vector from Gene Universal Inc. USA.

    Produced:

    Article Title: Deep learning-enabled scaffolding of spatial arrays of PfCSP epitopes
    Article Snippet: KDs were measured using n-Curve KinExA Analysis method provided in KinExA Pro software and described in Technology Note 229. .. To perform KinExA equilibrium experiments, the following materials were prepared: Constant Binding Partner (CBP), human IgG or Fab, was produced in Schief Lab; antigen was expressed and purified in Schief Lab; labeling antibody for IgG was Alexa Fluor 647 conjugated AffiniPure Goat Anti-HumanIgG, Fc Fragment Specific, Jackson ImmunoResearch code 109-605-008, 500 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at −80C); for Fab the labeling antibody was Alexa Fluor 647 conjugated AffiniPure Fab Fragment Goat Anti-Human IgG (H+L), Jackson ImmunoResearch code 109-607-003, 1000 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at - 20C); running buffer was the same as sample buffer and it was 1x HBS-EP+ pH 7.4 (20x stock from Teknova, Cat. No H8022) supplemented with BSA from Sigma (cat. A3294) at 1mg/ml; beads were Thermo Scientific UltraLink azlactone-activated, beaded-polyacrylamide resin cat. number 53110 and antigen was used as a cross-linked capturing reagent; and the instrument was KinExA 3200 with Autosampler model SAPIDYNE-AIM3300 (Sapidyne Instruments). ..

    Purification:

    Article Title: Deep learning-enabled scaffolding of spatial arrays of PfCSP epitopes
    Article Snippet: KDs were measured using n-Curve KinExA Analysis method provided in KinExA Pro software and described in Technology Note 229. .. To perform KinExA equilibrium experiments, the following materials were prepared: Constant Binding Partner (CBP), human IgG or Fab, was produced in Schief Lab; antigen was expressed and purified in Schief Lab; labeling antibody for IgG was Alexa Fluor 647 conjugated AffiniPure Goat Anti-HumanIgG, Fc Fragment Specific, Jackson ImmunoResearch code 109-605-008, 500 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at −80C); for Fab the labeling antibody was Alexa Fluor 647 conjugated AffiniPure Fab Fragment Goat Anti-Human IgG (H+L), Jackson ImmunoResearch code 109-607-003, 1000 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at - 20C); running buffer was the same as sample buffer and it was 1x HBS-EP+ pH 7.4 (20x stock from Teknova, Cat. No H8022) supplemented with BSA from Sigma (cat. A3294) at 1mg/ml; beads were Thermo Scientific UltraLink azlactone-activated, beaded-polyacrylamide resin cat. number 53110 and antigen was used as a cross-linked capturing reagent; and the instrument was KinExA 3200 with Autosampler model SAPIDYNE-AIM3300 (Sapidyne Instruments). ..

    Labeling:

    Article Title: Deep learning-enabled scaffolding of spatial arrays of PfCSP epitopes
    Article Snippet: KDs were measured using n-Curve KinExA Analysis method provided in KinExA Pro software and described in Technology Note 229. .. To perform KinExA equilibrium experiments, the following materials were prepared: Constant Binding Partner (CBP), human IgG or Fab, was produced in Schief Lab; antigen was expressed and purified in Schief Lab; labeling antibody for IgG was Alexa Fluor 647 conjugated AffiniPure Goat Anti-HumanIgG, Fc Fragment Specific, Jackson ImmunoResearch code 109-605-008, 500 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at −80C); for Fab the labeling antibody was Alexa Fluor 647 conjugated AffiniPure Fab Fragment Goat Anti-Human IgG (H+L), Jackson ImmunoResearch code 109-607-003, 1000 ng/ml in running buffer (prepared fresh from 1000x concentrated stock that is stored at - 20C); running buffer was the same as sample buffer and it was 1x HBS-EP+ pH 7.4 (20x stock from Teknova, Cat. No H8022) supplemented with BSA from Sigma (cat. A3294) at 1mg/ml; beads were Thermo Scientific UltraLink azlactone-activated, beaded-polyacrylamide resin cat. number 53110 and antigen was used as a cross-linked capturing reagent; and the instrument was KinExA 3200 with Autosampler model SAPIDYNE-AIM3300 (Sapidyne Instruments). ..

    Incubation:

    Article Title: Preclinical Characterization of XB002, an Anti–Tissue Factor Antibody–Drug Conjugate for the Treatment of Solid Tumors
    Article Snippet: .. After incubation, the plates were washed and incubated with peroxidase AffiniPure Goat Anti-Human IgG, Fc Fragment Specific (Jackson ImmunoResearch). .. Following another wash, horseradish peroxidase substrate (SuperSignal ELISA Pico Chemiluminescent substrate, Thermo Fisher Scientific) was added, and luminescence was measured using a plate reader spectrophotometer.

    Activation Assay:

    Article Title: Gremlin-1 inhibitor for the treatment of a bone fracture or bone defect
    Article Snippet: .. The capture ligand (affinipure F(ab′)2 fragment of goat anti-mouse IgG, Fc fragment specific, 115-006-071, Jackson ImmunoResearch Inc.) was immobilised at 50 μg/ml in 10 mM NaAc, pH5.0 on flow cell 2 of a CM4 Sensor Chip via amine coupling chemistry, using 600 s activation and deactivation injections, to a level of ̃1600 response units (RU). ..

    Article Title: Gremlin-1 crystal structure and inhibitory antibody
    Article Snippet: .. The capture ligand (affinipure F(ab′)2 fragment of goat anti-mouse IgG, Fc fragment specific, 115-006-071, Jackson ImmunoResearch Inc.) was immobilised at 50p g/ml in 10 mM NaAc, pH5.0 on flow cell 2 of a CM4 Sensor Chip via amine coupling chemistry, using 600s activation and deactivation injections, to a level of ̃1600 response units (RU). ..

    Saline:

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: Adalimumab, a humanized IgG1 monoclonal antibody is currently used to treat inflammatory diseases.. However, a sensitive, in-house ELISA for evaluating interand intra-individual pharmacokinetic variability of adalimumab remains limited.. In this study, an ELISA was developed to measure adalimumab levels, using recombinant human TNF-α (rhTNF-α) as capture antibody.

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: .. Nde-I and BamH-I (New England Biolabs Inc., UK), adalimumab (Humira®, AbbVie, USA), microtiter costar high binding 96-well assay plates (Corning Inc., USA), skimmed milk, tryptone type-II, 3-[(3-Cholamidopropyl) dimethylammonio]-1-propane sulfonate, LB Media and Tris-Cl (Hi-Media Laboratories, India), Tween-20, IPTG, human serum matrix (Sigma Aldrich, USA), kanamycin (Calbiochem, USA), peroxidase-conjugated goat anti-human IgG specific for Fc fragment (Jackson ImmunoResearch Cat# 109-035-008), 1X phosphate-buffered saline (1X PBS), and tetramethyl benzidine (20X TMB) (Denovo Biolabs, India), Ni-NTA column in AKTA (GE-AKTASTART, Cytiva, Sweden), surface plasma resonance (SPR) and 1-ethyl-3-(3-dimethylaminopropyl) (N-hydroxy succinimide) carbodiimide in combination with N-hydroxy succinimide (EDC-NHS) (Affinite, Canada), were procured for the study. .. The rhTNF-α used as coating reagent in ELISA was commercially cloned using pET28 a (+) vector from Gene Universal Inc. USA.

    Clinical Proteomics:

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: Adalimumab, a humanized IgG1 monoclonal antibody is currently used to treat inflammatory diseases.. However, a sensitive, in-house ELISA for evaluating interand intra-individual pharmacokinetic variability of adalimumab remains limited.. In this study, an ELISA was developed to measure adalimumab levels, using recombinant human TNF-α (rhTNF-α) as capture antibody.

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: .. Nde-I and BamH-I (New England Biolabs Inc., UK), adalimumab (Humira®, AbbVie, USA), microtiter costar high binding 96-well assay plates (Corning Inc., USA), skimmed milk, tryptone type-II, 3-[(3-Cholamidopropyl) dimethylammonio]-1-propane sulfonate, LB Media and Tris-Cl (Hi-Media Laboratories, India), Tween-20, IPTG, human serum matrix (Sigma Aldrich, USA), kanamycin (Calbiochem, USA), peroxidase-conjugated goat anti-human IgG specific for Fc fragment (Jackson ImmunoResearch Cat# 109-035-008), 1X phosphate-buffered saline (1X PBS), and tetramethyl benzidine (20X TMB) (Denovo Biolabs, India), Ni-NTA column in AKTA (GE-AKTASTART, Cytiva, Sweden), surface plasma resonance (SPR) and 1-ethyl-3-(3-dimethylaminopropyl) (N-hydroxy succinimide) carbodiimide in combination with N-hydroxy succinimide (EDC-NHS) (Affinite, Canada), were procured for the study. .. The rhTNF-α used as coating reagent in ELISA was commercially cloned using pET28 a (+) vector from Gene Universal Inc. USA.

    SPR Assay:

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: Adalimumab, a humanized IgG1 monoclonal antibody is currently used to treat inflammatory diseases.. However, a sensitive, in-house ELISA for evaluating interand intra-individual pharmacokinetic variability of adalimumab remains limited.. In this study, an ELISA was developed to measure adalimumab levels, using recombinant human TNF-α (rhTNF-α) as capture antibody.

    Article Title: Development and validation of a recombinant human TNF-α based ELISA to detect and quantify adalimumab
    Article Snippet: .. Nde-I and BamH-I (New England Biolabs Inc., UK), adalimumab (Humira®, AbbVie, USA), microtiter costar high binding 96-well assay plates (Corning Inc., USA), skimmed milk, tryptone type-II, 3-[(3-Cholamidopropyl) dimethylammonio]-1-propane sulfonate, LB Media and Tris-Cl (Hi-Media Laboratories, India), Tween-20, IPTG, human serum matrix (Sigma Aldrich, USA), kanamycin (Calbiochem, USA), peroxidase-conjugated goat anti-human IgG specific for Fc fragment (Jackson ImmunoResearch Cat# 109-035-008), 1X phosphate-buffered saline (1X PBS), and tetramethyl benzidine (20X TMB) (Denovo Biolabs, India), Ni-NTA column in AKTA (GE-AKTASTART, Cytiva, Sweden), surface plasma resonance (SPR) and 1-ethyl-3-(3-dimethylaminopropyl) (N-hydroxy succinimide) carbodiimide in combination with N-hydroxy succinimide (EDC-NHS) (Affinite, Canada), were procured for the study. .. The rhTNF-α used as coating reagent in ELISA was commercially cloned using pET28 a (+) vector from Gene Universal Inc. USA.

    Membrane:

    Article Title: Fully human antibody targeting CD19 and application thereof
    Article Snippet: The brief experimental steps are as follows: 1) MPA contains about 5000 different membrane protein clones, accounting for more than 90% of the human membrane proteome, with each clone overexpressed in HEK-293T cells comprising a cDNA plasmid, and the plasmid was independently used for transfection in separate wells of a 384-well cell culture plate, with an incubation time of 36 h to ensure the expression of membrane proteins; 2) prior to specificity test on MPA, determine the test concentrations of antibody #78 for screening on HEK-293T and QT6 cells expressing positive (ProteinA) and negative (mock transfection) controls by flow cytometry using AlexaFluor 647-labelled secondary antibody; 3) dilute Clone 78 antibody to 20 μg/mL and test the entire protein library for binding activity using the above secondary antibody on IntellicytiQue; to ensure plate-to-plate compatibility and repeatability, include both positive and negative controls for each array plate; and 4) after serial dilution of antibody #78, reconfirm whether each target determined by MPA screening can bind in a repeatable and dose-dependent manner by another flow cytometry assay, and verify the identity of the target by sequencing. .. Main Samples and Reagents: Cell lines: HEK-293T, Q6T Alexa Fluor target identity Affiniti Pure F (ab′) 2 Fragment Goat Anti-Rabbit IgG, Fc fragment specific, Jackson ImmunoResearch, 111-606-046 Goat Serum, Sigma, G6767 Experimental Results: As shown in FIG. 16, during the preliminary screening stage of the test, antibody #78 did not specifically bind to most of the 5000 membrane proteins, but bound to HEK-293T cells with high expression of SDC1, Fizzled 4 and HTR5A. .. To verify the repeatability of this binding, we diluted the antibody #78 with a concentration gradient and repeated the experiment, which showed that the antibody #78 could bind to HEK-293T cells with high expression of CD19 and the positive control (ProteinA), and the mean fluorescence intensity of its binding was dose-dependent.

    Expressing:

    Article Title: Fully human antibody targeting CD19 and application thereof
    Article Snippet: The brief experimental steps are as follows: 1) MPA contains about 5000 different membrane protein clones, accounting for more than 90% of the human membrane proteome, with each clone overexpressed in HEK-293T cells comprising a cDNA plasmid, and the plasmid was independently used for transfection in separate wells of a 384-well cell culture plate, with an incubation time of 36 h to ensure the expression of membrane proteins; 2) prior to specificity test on MPA, determine the test concentrations of antibody #78 for screening on HEK-293T and QT6 cells expressing positive (ProteinA) and negative (mock transfection) controls by flow cytometry using AlexaFluor 647-labelled secondary antibody; 3) dilute Clone 78 antibody to 20 μg/mL and test the entire protein library for binding activity using the above secondary antibody on IntellicytiQue; to ensure plate-to-plate compatibility and repeatability, include both positive and negative controls for each array plate; and 4) after serial dilution of antibody #78, reconfirm whether each target determined by MPA screening can bind in a repeatable and dose-dependent manner by another flow cytometry assay, and verify the identity of the target by sequencing. .. Main Samples and Reagents: Cell lines: HEK-293T, Q6T Alexa Fluor target identity Affiniti Pure F (ab′) 2 Fragment Goat Anti-Rabbit IgG, Fc fragment specific, Jackson ImmunoResearch, 111-606-046 Goat Serum, Sigma, G6767 Experimental Results: As shown in FIG. 16, during the preliminary screening stage of the test, antibody #78 did not specifically bind to most of the 5000 membrane proteins, but bound to HEK-293T cells with high expression of SDC1, Fizzled 4 and HTR5A. .. To verify the repeatability of this binding, we diluted the antibody #78 with a concentration gradient and repeated the experiment, which showed that the antibody #78 could bind to HEK-293T cells with high expression of CD19 and the positive control (ProteinA), and the mean fluorescence intensity of its binding was dose-dependent.



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