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rabbit anti human il 22r1 polyclonal antibodies  (ProSci Incorporated)


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    Structured Review

    ProSci Incorporated rabbit anti human il 22r1 polyclonal antibodies
    Figure 4. Interleukin-22 receptor 1 <t>(IL-22R1)</t> mRNA expression in rheumatoid arthritis (RA) synovial tissues. Reverse transcription– polymerase chain reaction for IL-22R1 or -actin was performed using mRNA extracted from the synovial tissues of 4 RA patients (RA1– RA4). Hep-G2 cells were used as a positive control.
    Rabbit Anti Human Il 22r1 Polyclonal Antibodies, supplied by ProSci Incorporated, 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/rabbit+anti+human+il+22r1+polyclonal+antibodies/IL-22+Receptor+Antibody/pm15818686-80-0-7
    Average 90 stars, based on 1 article reviews
    rabbit anti human il 22r1 polyclonal antibodies - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine."

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.

    Journal: Arthritis and rheumatism

    doi: 10.1002/art.20965

    Figure 4. Interleukin-22 receptor 1 (IL-22R1) mRNA expression in rheumatoid arthritis (RA) synovial tissues. Reverse transcription– polymerase chain reaction for IL-22R1 or -actin was performed using mRNA extracted from the synovial tissues of 4 RA patients (RA1– RA4). Hep-G2 cells were used as a positive control.
    Figure Legend Snippet: Figure 4. Interleukin-22 receptor 1 (IL-22R1) mRNA expression in rheumatoid arthritis (RA) synovial tissues. Reverse transcription– polymerase chain reaction for IL-22R1 or -actin was performed using mRNA extracted from the synovial tissues of 4 RA patients (RA1– RA4). Hep-G2 cells were used as a positive control.

    Techniques Used: Expressing, Reverse Transcription, Polymerase Chain Reaction, Positive Control

    Figure 5. Immunohistologic localization of IL-22R1 in synovial tissue from either patients with RA (A and C–J) or patients with osteoar- thritis (B). Dual-labeling immunofluorescence staining of RA synovial tissues (C–J) was done with anti–IL-22R1 (green) (C and G), anti- vimentin (red) (D), and anti-CD68 (red) (H). Staining of nuclei was done with 4,6-diamidino-2-phenylindole (blue) (E and I). Merged images are shown in F (merger of C, D, and E) and J (merger of G, H, and I). See Figure 4 for definitions. (Counterstained with hematoxylin; original magnification 200.)
    Figure Legend Snippet: Figure 5. Immunohistologic localization of IL-22R1 in synovial tissue from either patients with RA (A and C–J) or patients with osteoar- thritis (B). Dual-labeling immunofluorescence staining of RA synovial tissues (C–J) was done with anti–IL-22R1 (green) (C and G), anti- vimentin (red) (D), and anti-CD68 (red) (H). Staining of nuclei was done with 4,6-diamidino-2-phenylindole (blue) (E and I). Merged images are shown in F (merger of C, D, and E) and J (merger of G, H, and I). See Figure 4 for definitions. (Counterstained with hematoxylin; original magnification 200.)

    Techniques Used: Labeling, Immunofluorescence, Staining

    Figure 6. Expression of IL-22 (A) and IL-22R1 (B and C) in synovial fibroblasts established from RA tissues (RASF) obtained from 4 RA patients (RA1–RA4). Reverse transcription–polymerase chain reac- tion for IL-22 (A), IL-22R1 (B), or -actin was performed using mRNA extracted from RASF. Western blotting was performed using specific antibodies against IL-22R1 (C). Peripheral blood mono- nuclear cells from normal donors, stimulated with phytohemagglutinin (PC) or without phytohemagglutinin (NC), were used as positive and negative controls, respectively (A). Hep-G2 was used as a positive control for IL-22R1 (B and C). See Figure 4 for other definitions.
    Figure Legend Snippet: Figure 6. Expression of IL-22 (A) and IL-22R1 (B and C) in synovial fibroblasts established from RA tissues (RASF) obtained from 4 RA patients (RA1–RA4). Reverse transcription–polymerase chain reac- tion for IL-22 (A), IL-22R1 (B), or -actin was performed using mRNA extracted from RASF. Western blotting was performed using specific antibodies against IL-22R1 (C). Peripheral blood mono- nuclear cells from normal donors, stimulated with phytohemagglutinin (PC) or without phytohemagglutinin (NC), were used as positive and negative controls, respectively (A). Hep-G2 was used as a positive control for IL-22R1 (B and C). See Figure 4 for other definitions.

    Techniques Used: Expressing, Reverse Transcription, Western Blot, Positive Control

    Related Articles

    Expressing:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).

    Reverse Transcription:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).

    Polymerase Chain Reaction:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).

    Positive Control:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).

    Labeling:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).

    Immunofluorescence:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).

    Staining:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).

    Western Blot:

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.
    Article Snippet: Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).Goat anti-human IL-22 polyclonal antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA).. Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).. Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).Mouse anti-CD3 monoclonal antibodies were from Nichirei (Tokyo, Japan).



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    ProSci Incorporated rabbit anti human il 22r1 polyclonal antibodies
    Figure 4. Interleukin-22 receptor 1 <t>(IL-22R1)</t> mRNA expression in rheumatoid arthritis (RA) synovial tissues. Reverse transcription– polymerase chain reaction for IL-22R1 or -actin was performed using mRNA extracted from the synovial tissues of 4 RA patients (RA1– RA4). Hep-G2 cells were used as a positive control.
    Rabbit Anti Human Il 22r1 Polyclonal Antibodies, supplied by ProSci Incorporated, 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/rabbit+anti+human+il+22r1+polyclonal+antibodies/IL-22+Receptor+Antibody/pm15818686-80-0-7
    Average 90 stars, based on 1 article reviews
    rabbit anti human il 22r1 polyclonal antibodies - by Bioz Stars, 2026-09
    90/100 stars
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    Figure 4. Interleukin-22 receptor 1 (IL-22R1) mRNA expression in rheumatoid arthritis (RA) synovial tissues. Reverse transcription– polymerase chain reaction for IL-22R1 or -actin was performed using mRNA extracted from the synovial tissues of 4 RA patients (RA1– RA4). Hep-G2 cells were used as a positive control.

    Journal: Arthritis and rheumatism

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.

    doi: 10.1002/art.20965

    Figure Lengend Snippet: Figure 4. Interleukin-22 receptor 1 (IL-22R1) mRNA expression in rheumatoid arthritis (RA) synovial tissues. Reverse transcription– polymerase chain reaction for IL-22R1 or -actin was performed using mRNA extracted from the synovial tissues of 4 RA patients (RA1– RA4). Hep-G2 cells were used as a positive control.

    Article Snippet: Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).

    Techniques: Expressing, Reverse Transcription, Polymerase Chain Reaction, Positive Control

    Figure 5. Immunohistologic localization of IL-22R1 in synovial tissue from either patients with RA (A and C–J) or patients with osteoar- thritis (B). Dual-labeling immunofluorescence staining of RA synovial tissues (C–J) was done with anti–IL-22R1 (green) (C and G), anti- vimentin (red) (D), and anti-CD68 (red) (H). Staining of nuclei was done with 4,6-diamidino-2-phenylindole (blue) (E and I). Merged images are shown in F (merger of C, D, and E) and J (merger of G, H, and I). See Figure 4 for definitions. (Counterstained with hematoxylin; original magnification 200.)

    Journal: Arthritis and rheumatism

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.

    doi: 10.1002/art.20965

    Figure Lengend Snippet: Figure 5. Immunohistologic localization of IL-22R1 in synovial tissue from either patients with RA (A and C–J) or patients with osteoar- thritis (B). Dual-labeling immunofluorescence staining of RA synovial tissues (C–J) was done with anti–IL-22R1 (green) (C and G), anti- vimentin (red) (D), and anti-CD68 (red) (H). Staining of nuclei was done with 4,6-diamidino-2-phenylindole (blue) (E and I). Merged images are shown in F (merger of C, D, and E) and J (merger of G, H, and I). See Figure 4 for definitions. (Counterstained with hematoxylin; original magnification 200.)

    Article Snippet: Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).

    Techniques: Labeling, Immunofluorescence, Staining

    Figure 6. Expression of IL-22 (A) and IL-22R1 (B and C) in synovial fibroblasts established from RA tissues (RASF) obtained from 4 RA patients (RA1–RA4). Reverse transcription–polymerase chain reac- tion for IL-22 (A), IL-22R1 (B), or -actin was performed using mRNA extracted from RASF. Western blotting was performed using specific antibodies against IL-22R1 (C). Peripheral blood mono- nuclear cells from normal donors, stimulated with phytohemagglutinin (PC) or without phytohemagglutinin (NC), were used as positive and negative controls, respectively (A). Hep-G2 was used as a positive control for IL-22R1 (B and C). See Figure 4 for other definitions.

    Journal: Arthritis and rheumatism

    Article Title: Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine.

    doi: 10.1002/art.20965

    Figure Lengend Snippet: Figure 6. Expression of IL-22 (A) and IL-22R1 (B and C) in synovial fibroblasts established from RA tissues (RASF) obtained from 4 RA patients (RA1–RA4). Reverse transcription–polymerase chain reac- tion for IL-22 (A), IL-22R1 (B), or -actin was performed using mRNA extracted from RASF. Western blotting was performed using specific antibodies against IL-22R1 (C). Peripheral blood mono- nuclear cells from normal donors, stimulated with phytohemagglutinin (PC) or without phytohemagglutinin (NC), were used as positive and negative controls, respectively (A). Hep-G2 was used as a positive control for IL-22R1 (B and C). See Figure 4 for other definitions.

    Article Snippet: Rabbit anti-human IL-22R1 polyclonal antibodies were from Prosci Incorporated (Poway, CA).

    Techniques: Expressing, Reverse Transcription, Western Blot, Positive Control