HIGH PERFORMANCE ANTIBODIES … AND MORE

Infectious Disease

Infectious Disease Research

Infectious diseases result from a host being exposed to a pathogen such as bacteria or viruses. Antibodies can be used to detect these pathogens or key targets that these pathogens use to infect a host. Antibodies can also be used to better treat and understand the diseases caused by these pathogens. ProSci offers various antibodies to aid researchers to have a better understanding of how to detect and treat infectious diseases.

View Infectious Disease Research Reagents

    Primary Antibodies

  • ACE2 Antibody

    Catalog Number: 3215

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    9 Image(s)

    • <strong>Figure 1 Independent Antibody Validation (IAV) via Protein Expression Profile in Human Tissues</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3215 (2 μg/mL), ACE2, 3217 (2 μg/mL), ACE2, 3227 (2 μg/mL) and beta-actin 3779 (1 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 2 Western Blot Validation in Human Tissues</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3215 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 3 Western Blot Validation in Mouse Tissues</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3215 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 4 Western Blot Validation in Rat Skin Tissue</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3215 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 5 Immunohistochemistry Validation of ACE2 in Human Kidney Tissue </strong><br> Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-ACE2 antibody (3215) at 2 μg/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4˚C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.
    • <strong>Figure 6 Immunofluorescence Validation of ACE2 in Human Testis Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human testis tissue labeling ACE-2 with 3215 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 7 Immunofluorescence Validation of ACE2 in Human Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human lung tissue labeling ACE-2 with 3215 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 8 Immunofluorescence Validation of ACE2 in Rat Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed rat lung tissue labeling ACE-2 with 3215 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 9 Immunofluorescence Validation of ACE2 In Caco2 Cells </strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed Caco2 cells labeling ACE2 with 3215 at 20 ug/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue). Image showing membrane staining on Caco2 cells.

  • ACE2 Antibody

    Catalog Number: 3217

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    11 Image(s)

    • <strong>Figure 1 Independent Antibody Validation (IAV) via Protein Expression Profile in Human Tissues</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3215 (2 μg/mL), ACE2, 3217 (2 μg/mL), ACE2, 3217 (2 μg/mL) and beta-actin 3779 (1 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 2 Western Blot Validation in Human Tissues and Cell Line</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3217 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 3 Western Blot Validation in Mouse Tissues </strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3217 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 4 Western Blot Validation in Rat Tissues </strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3217 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 5 Immunofluorescence Validation of ACE2 in Human Testis Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human testis tissue labeling ACE-2 with 3217 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 6 Immunofluorescence Validation of ACE2 in Human Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human lung tissue labeling ACE-2 with 3217 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 7 Immunofluorescence Validation of ACE2 in Mouse Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse lung tissue labeling ACE-2 with 3217 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 8 Immunofluorescence Validation of ACE2 in Rat Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed rat lung tissue labeling ACE-2 with 3217 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 9 Immunohistochemistry Validation of ACE2 in Human Kidney Tissue </strong><br> Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-ACE2 antibody (3217) at 2 μg/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4˚C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.
    • <strong>Figure 10 Immunofluorescence Validation of ACE2 in Human Kidney Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human kidney cells labeling ACE2 with 3217 at 10 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (red).
    • <strong>Figure 11 Immunofluorescence Validation of ACE2 In Caco2 Cells </strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed Caco2 cells labeling ACE2 with 3217 at 5 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue). Image showing membrane staining on Caco2 cells.

  • ACE2 Antibody

    Catalog Number: 3227

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    11 Image(s)

    • <strong>Figure 1 Independent Antibody Validation (IAV) via Protein Expression Profile in Human Tissues</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3215 (2 μg/mL), ACE2, 3217 (2 μg/mL), ACE2, 3227 (2 μg/mL) and beta-actin 3779 (1 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 2 Western Blot Validation in Human Tissues</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3227 (1 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 3 Western Blot Validation in Mouse Tissues</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3227 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 4 Western Blot Validation in Rat Thymus Tissue</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3227 (2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 5 Immunohistochemistry Validation of ACE2 in Human Kidney Tissue </strong><br> Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-ACE2 antibody (3227) at 2 μg/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4 ˚C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.
    • <strong>Figure 6 Immunofluorescence Validation of ACE2 in Human Testis Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human testis tissue labeling ACE-2 with 3227 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 7 Immunofluorescence Validation of ACE2 in Human Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human lung tissue labeling ACE-2 with 3227 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 8 Immunofluorescence Validation of ACE2 in Mouse Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse lung tissue labeling ACE-2 with 3227 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 9 Immunofluorescence Validation of ACE2 in Rat Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed rat lung tissue labeling ACE-2 with 3227 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 10 Immunofluorescence Validation of ACE2 in Human Kidney Cells</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human kidney cells labeling ACE2 with 3227 at 10 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (red).
    • <strong>Figure 11 Immunofluorescence Validation of ACE2 In Caco2 Cells </strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed Caco2 cells labeling ACE2 with 3227 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue). Image showing membrane staining on Caco2 cells.

  • ACE2 Antibody

    Catalog Number: 3229

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    10 Image(s)

    • <strong>Figure 1 Western Blot Validation in Human Tissues</strong><br> Loading: 15 µg of lysates per lane. Antibodies: ACE2, 3229 (4 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 2 Western Blot Validation in Mouse Stomach Tissue</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3229 (4 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 3 Western Blot Validation in Rat Brain Tissue</strong><br> Loading: 15 μg of lysates per lane. Antibodies: ACE2, 3229 (4 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 4 Immunohistochemistry Validation of ACE2 in Human Kidney Tissue </strong><br> Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-ACE2 antibody (3229) at 2 μg/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4 ˚C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.
    • <strong>Figure 5 Immunofluorescence Validation of ACE2 in Human Kidney Cells</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human kidney cells labeling ACE2 with 3229 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green).
    • <strong>Figure 6 Immunofluorescence Validation of ACE2 in Human Testis Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human testis tissue labeling ACE-2 with 3229 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 7 Immunofluorescence Validation of ACE2 in Human Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human lung tissue labeling ACE-2 with 3229 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 8 Immunofluorescence Validation of ACE2 in Mouse Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse lung tissue labeling ACE-2 with 3229 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 9 Immunofluorescence Validation of ACE2 in Rat Lung Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed rat lung tissue labeling ACE-2 with 3229 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 10 Immunofluorescence Validation of ACE2 In Caco2 Cells </strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed Caco2 cells labeling ACE2 with 3229 at 5 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue). Image showing membrane staining on Caco2 cells.

  • ATR Antibody

    Catalog Number: 3117

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    3 Image(s)

    • Western blot analysis of ATR in HepG2 cell lysates with ATR antibody (IN) at (A) 0.5, (B) 1, and (C) 2 μg/mL.
    • Immunohistochemical staining of human brain tissue using ATR antibody at 2 μg/mL.
    • Immunofluorescence of ATR in Human Brain tissue with ATR antibody at 10 ug/mL.

  • CAPN6 Antibody

    Catalog Number: 4759

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    3 Image(s)

    • Western blot analysis of CAPN6 in rat lung tissue lysate with CAPN6 antibody at (A) 0.5 and (B) 1 μg/mL.
    • Immunohistochemistry of CAPN6 in human lung tissue with CAPN6 antibody at 2.5 μg/mL.
    • Immunofluorescence of CAPN6 in Human Lung cells with CAPN6 antibody at 20 μg/mL.

  • CCR3 Antibody

    Catalog Number: 1105

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    3 Image(s)

    • Western blot analysis of CCR3 in human spleen tissue lysates with CCR3 antibody at 1 (lane 1) and 2 μg/mL (lane 2), and 2 μg/mL in the presence of blocking peptide (lane 3).
    • Immunohistochemistry of CCR3 in human spleen tissue with CCR3 antibody at 10 μg/mL.
    • Immunofluorescence of CCR3 in Human Spleen tissue with CCR3 antibody at 20 μg/mL.

  • CD81 Antibody

    Catalog Number: 5195

    Clonality: Polyclonal

    Tested Applications: ELISA, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    5 Image(s)

    • Western blot analysis of CD81 in human lung tissue lysate with CD81 antibody at 1 μg/mL in (A) the absence and (B) the presence of blocking petide.
    • Immunohistochemistry of CD81 in human lung tissue with CD81 antibody at 5 μg/mL.
    • Immunofluorescence of CD81 in A549 cells with CD81 antibody at 20 μg/mL.
    • Immunohistochemistry of CD81 in human brain tissue with CD81 antibody at 2 μg/ml.
    • Immunofluorescence of CD81 in human brain tissue with CD81 antibody at 10 μg/ml.<br><br>Green: CD81 Antibody (5195) <br> Blue: DAPI staining

  • CD81 Antibody [1.3.3.22]

    Catalog Number: 33-829

    Clonality: Monoclonal

    Tested Applications: Flow, Func, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Mouse

    Conjugate: Unconjugated

    Size: 100 ug

    2 Image(s)

    • IHC testing of FFPE human lymph node with CD81 antibody (clone 1.3.3.22). Required HIER: boil tissue sections in 10mM citrate buffer, pH 6, for 10-20 min followed by cooling at RT for 20 min.
    • IHC testing of FFPE human tonsil with CD81 antibody (clone 1.3.3.22). Required HIER: boil tissue sections in 10mM citrate buffer, pH 6, for 10-20 min followed by cooling at RT for 20 min.

  • CX3CR1 Antibody

    Catalog Number: 2093

    Clonality: Polyclonal

    Tested Applications: ELISA, Flow, IF, IHC-P, WB

    Species Reactivity: Human, Mouse, Rat

    Host Species: Rabbit

    Conjugate: Unconjugated

    Size: 0.02 mg, 0.1 mg

    15 Image(s)

    • <strong>Figure 1 Western Blot Validation in Human Cells </strong><br> Loading: 15 μg of lysates per lane. Antibodies: CX3CR1 2093 (0.5 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 2 KD Validation in 293 Cells</strong><br> Loading: 15 μg of lysates per lane. Antibodies: CX3CR1 2093 (0.5 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution. Lane 1: 293 cells transfected with control siRNAs. Lane 2: 293 cells transfected with CX3CR1 siRNAs.
    • <strong>Figure 3 Western Blot Validation in THP1 Cells </strong><br> Loading: 15 μg of lysates per lane. Antibodies: CX3CR1 2093 (1 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution. Lane 1: 0.2 μg/mL Lane 1: 0.5 μg/mL Lane 1: 1 μg/mL
    • <strong>Figure 4 Western Blot Validation in Human Spleen Lysates</strong><br> Loading: 15 μg of lysates per lane. Antibodies: CX3CR1 2093 (1 μg/mL) in the absence (lane 1) or presence of blocking peptide (lane 2), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 5 Western Blot Validation in Rat Spleen Tissue</strong><br> Loading: 15 μg of lysates per lane. Antibodies: CX3CR1 2093, (A; 1 μg/mL, B; 2 μg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
    • <strong>Figure 6 Flow Cytometry Validation of CX3CR1 in THP-1 Cells</strong><br> Overlay histogram showing THP-1 cells stained with 2093 (red line, 1μg/1x10<sup>6</sup> cells). 1 h incubation at 4˚C in 2% FBS/PBS. Followed by secondary antibody 488 goat anti-rabbit IgG (H+L) at 1/500 dilution for 1 h 4˚C. <br> <br> Isotype control antibody (Green line) was rabbit IgG1 (1μg/1x10<sup>6</sup> cells) used under the same conditions. Acquisition of >10,000 events was performed.
    • <strong>Figure 7 Immunofluorescence Validation of CX3CR1 In K562 Cells </strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed K562 cells labeling CX3CR1 with 2093 at 10 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (red) and DAPI staining (blue). Image showing membrane staining on K562 cells.
    • <strong>Figure 8 Immunofluorescence Validation of CX3CR1 in Human Heart </strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed human heart tissue labeling CX3CR1 with 2093 at 10 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (red).
    • <strong>Figure 9 Immunofluorescence Validation of CX3CR1 in Mouse Heart Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed mouse heart tissue labeling CX3CR1 with 2093 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 10 Immunohistochemistry Validation of CX3CR1 in Rat Heart Tissue </strong><br> Immunohistochemical analysis of paraffin-embedded rat heart tissue using anti-CX3CR1 antibody (2093) at 2 μg/ml. Tissue was fixed with formaldehyde and blocked with 10% serum for 1 h at RT; antigen retrieval was by heat mediation with a citrate buffer (pH6). Samples were incubated with primary antibody overnight at 4˚C. A goat anti-rabbit IgG H&L (HRP) at 1/250 was used as secondary. Counter stained with Hematoxylin.
    • <strong>Figure 11 Immunofluorescence Validation of CX3CR1 in Rat Heart Tissue</strong><br> Immunofluorescent analysis of 4% paraformaldehyde-fixed rat heart tissue labeling CX3CR1 with 2093 at 20 μg/mL, followed by goat anti-rabbit IgG secondary antibody at 1/500 dilution (green) and DAPI staining (blue).
    • <strong>Figure 12 Immunofluorescence Validation of CX3CR1 in Human Atherosclerosis (Lucas et al., 2003)</strong><br> CX3CR1-positive cells in coronary artery sections was detected by anti-CX3CR1 antibodies by double staining with an anti–smooth muscle actin antibody (yellow).
    • <strong>Figure 13 Regulated Expression Validation of CX3CR1 in Mouse Bone Marrow-derived NK Cells (Barlic et al., 2003)</strong><br> Western blot analysis of CX3CR1 expression detected by anti-CX3CR1 antibodies was induced by IL-2 but was inhibited by IL-15. Mouse skeletal muscle was for negative control and mouse brain was for positive control.
    • <strong>Figure 14 Flow Cytometry Validation of CX3CR1 in Peripheral Blood Mononuclear Cells (PBMCs) of Patients (Yajima et al., 2005)</strong><br> Flow cytometry analysis of CX3CR1 expression detected by anti-CX3CR1 antibodies. Protein expression was more pronounced on CD4<sup>+</sup> and CD8<sup>+</sup> T cells from patients with untreated active systemic lupus erythematosus (SLE) as compared to those with rheumatoid arthritis (RA) or healthy controls.
    • <strong>Figure 15 CX3CR1 Deficiency Validation in Transgenic Mice (Kumar et al., 2013)</strong><br> Transgenic CX3CR1 gfp (C57BL6/J background) mice, in which either one (CX3CR1 gfp/+ ) or both (CX3CR1 gfp/gfp ) copies of the CX3CR1 gene were interrupted by fluorescent protein (GFP). More CX3CR1 positive cells (green) are found in vascular wall of CX3CR1 gfp/+ mice, but not in CX3CR1 gfp/gfp mice, where cells remained in perivascular region due to leaky microvessels. CX3CR1 expression was detected by anti-CX3CR1 antibodies.
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