Review



rabbit anti rat txnip  (Thermo Fisher)


Bioz Verified Symbol Thermo Fisher is a verified supplier
Bioz Manufacturer Symbol Thermo Fisher manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 94
      Buy from Supplier

    Structured Review

    Thermo Fisher rabbit anti rat txnip
    The expression of TNXIP in the lesioned spinal cord following compression was observed. ( A ) The TNXIP/NeuN expression in the anterior horn of lesioned spinal cords was analyzed by immunofluorescence. The mean fluorescence intensities of <t>TXNIP</t> were analyzed by Image J software, and represented as mean gray values. ( B ) The TXNIP expression in the lesioned spinal cords was analyzed by Western blot. The gray values of protein bands were analyzed by Image J software, and protein expression was normalized to GAPDH. *P<0.05, **P<0.01.
    Rabbit Anti Rat Txnip, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti rat txnip/product/Thermo Fisher
    Average 94 stars, based on 7 article reviews
    rabbit anti rat txnip - by Bioz Stars, 2026-03
    94/100 stars

    Images

    1) Product Images from "TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy"

    Article Title: TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy

    Journal: Journal of Inflammation Research

    doi: 10.2147/JIR.S373614

    The expression of TNXIP in the lesioned spinal cord following compression was observed. ( A ) The TNXIP/NeuN expression in the anterior horn of lesioned spinal cords was analyzed by immunofluorescence. The mean fluorescence intensities of TXNIP were analyzed by Image J software, and represented as mean gray values. ( B ) The TXNIP expression in the lesioned spinal cords was analyzed by Western blot. The gray values of protein bands were analyzed by Image J software, and protein expression was normalized to GAPDH. *P<0.05, **P<0.01.
    Figure Legend Snippet: The expression of TNXIP in the lesioned spinal cord following compression was observed. ( A ) The TNXIP/NeuN expression in the anterior horn of lesioned spinal cords was analyzed by immunofluorescence. The mean fluorescence intensities of TXNIP were analyzed by Image J software, and represented as mean gray values. ( B ) The TXNIP expression in the lesioned spinal cords was analyzed by Western blot. The gray values of protein bands were analyzed by Image J software, and protein expression was normalized to GAPDH. *P<0.05, **P<0.01.

    Techniques Used: Expressing, Immunofluorescence, Fluorescence, Software, Western Blot

    Inhibition of TXNIP improved CSM-induced behavioral deficits. ( A ) The21-point Basso, Beattie and Bresnahan (BBB) locomotor rating scale; ( B ) cold allodynia; ( C ) inclined plane test. Compared with the sham group, **P<0.01; compared with the scrambled group, # P<0.05, ## P<0.01.
    Figure Legend Snippet: Inhibition of TXNIP improved CSM-induced behavioral deficits. ( A ) The21-point Basso, Beattie and Bresnahan (BBB) locomotor rating scale; ( B ) cold allodynia; ( C ) inclined plane test. Compared with the sham group, **P<0.01; compared with the scrambled group, # P<0.05, ## P<0.01.

    Techniques Used: Inhibition

    Inhibition of TXNIP reduced apoptosis in the anterior horn of the lesioned area following CSM. ( A ) Positive TUNEL staining control. ( B ) Apoptosis in the anterior horn of the lesioned area was analyzed by TUNEL staining. Black arrows show apoptotic cells. Apoptosis rate (%) = the numbers of apoptosis cells/total numbers of cells ×100%. The numbers of cells were counted using Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.
    Figure Legend Snippet: Inhibition of TXNIP reduced apoptosis in the anterior horn of the lesioned area following CSM. ( A ) Positive TUNEL staining control. ( B ) Apoptosis in the anterior horn of the lesioned area was analyzed by TUNEL staining. Black arrows show apoptotic cells. Apoptosis rate (%) = the numbers of apoptosis cells/total numbers of cells ×100%. The numbers of cells were counted using Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Techniques Used: Inhibition, TUNEL Assay, Staining, Control, Software

    Inhibition of TXNIP declined the TXNIP expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of TXNIP/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed using Image J software. Compared with the sham group, *P<0.05, **P<0.01; compared with the scrambled group, ## P<0.01.
    Figure Legend Snippet: Inhibition of TXNIP declined the TXNIP expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of TXNIP/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed using Image J software. Compared with the sham group, *P<0.05, **P<0.01; compared with the scrambled group, ## P<0.01.

    Techniques Used: Inhibition, Expressing, Fluorescence, Immunofluorescence, Software

    Inhibition of TXNIP declined the NLRP3 expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of NLRP3/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed by Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.
    Figure Legend Snippet: Inhibition of TXNIP declined the NLRP3 expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of NLRP3/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed by Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Techniques Used: Inhibition, Expressing, Fluorescence, Immunofluorescence, Software

    Inhibition TXNIP declined the NLRP3 mediated pro-caspase-1 expression in the anterior horn of the lesioned area following CSM. ( A ) The mean fluorescence intensities of pro-caspase-1/NeuN were analyzed by immunofluorescence. ( B ) The expression levels of TXNIP, NLRP3 and pro-caspase-1 in the lesioned spinal cords were measured by Western blot. The mean grays were analyzed by the Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.
    Figure Legend Snippet: Inhibition TXNIP declined the NLRP3 mediated pro-caspase-1 expression in the anterior horn of the lesioned area following CSM. ( A ) The mean fluorescence intensities of pro-caspase-1/NeuN were analyzed by immunofluorescence. ( B ) The expression levels of TXNIP, NLRP3 and pro-caspase-1 in the lesioned spinal cords were measured by Western blot. The mean grays were analyzed by the Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Techniques Used: Inhibition, Expressing, Fluorescence, Immunofluorescence, Western Blot, Software



    Similar Products

    rabbit anti rat txnip  (Thermo Fisher)
    94
    Thermo Fisher rabbit anti rat txnip
    The expression of TNXIP in the lesioned spinal cord following compression was observed. ( A ) The TNXIP/NeuN expression in the anterior horn of lesioned spinal cords was analyzed by immunofluorescence. The mean fluorescence intensities of <t>TXNIP</t> were analyzed by Image J software, and represented as mean gray values. ( B ) The TXNIP expression in the lesioned spinal cords was analyzed by Western blot. The gray values of protein bands were analyzed by Image J software, and protein expression was normalized to GAPDH. *P<0.05, **P<0.01.
    Rabbit Anti Rat Txnip, supplied by Thermo Fisher, 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/result/rabbit anti rat txnip/product/Thermo Fisher
    Average 94 stars, based on 1 article reviews
    rabbit anti rat txnip - by Bioz Stars, 2026-03
    94/100 stars
    		  Buy from Supplier
    rabbit anti rat txnip  (Abcam)
    98
    Abcam rabbit anti rat txnip
    The impact of ROS and NLRP3 inflammasome on the expression of pyroptosis associated gene and protein. (A)The gene and protein expression of <t>TXNIP,</t> NLRP3, and Caspae-1 in NRK-52E cells under 200 μg/ml uric acid stimulation or not for 24 hr detected by Real-time PCR and western blot techniques (n=3). The cells were categorized into four groups: the control group (0 μg/ml uric acid), the UA group (200 μg/ml uric), the UA+ROS (−) group (200 μg/ml uric + the ROS inhibitors NAC), as well as the UA+mtROS (−) group (200 μg/ml uric+ mtROS inhibitors mt-TEMPO). Data were expressed as mean ± SD. Compared with the UA group, ** P < 0.0001, * P < 0.05. Compared with the UA+ROS (−) group, ⋆⋆ P < 0.0001, ⋆ P < 0.05. Compared with UA+mtROS(−) group, # # P < 0.0001, # P < 0.05.(B) The pyroptosis percent in NRK-52E cells subjected to 200 μg/ml uric acid or not for 24 hr via flow cytometry method (n=3). The cells were divided into four groups: the control group (0 μg/ml uric acid), the UA group (200 μg/ml uric), the UA+NLRP3 (−) group (200 μg/ml uric + the NLRP3 inhibitors MCC950), <t>the</t> <t>UA+Caspase-1(−)</t> group (200 μg/ml uric+ Caspase-1 inhibitors Z-YVAD-FMK). Data were expressed as mean ± SD. Compared with the UA group, ** P < 0.0001, * P < 0.05. Compared with the UA+NLRP3 (-) group, ⋆⋆ P < 0.0001, ⋆ P < 0.05. Compared with UA+Caspase-1(−) group, ## P < 0.0001, # P < 0.05.(C) The gene and protein expression of NLRP3, ASC, Caspae-1, Activated-Caspase-1, GSDMD, IL-1β, and IL-18 in NRK-52E cells when exposed to 200 μg/ml uric acid or not for 24 hr using Real-time PCR and western blot method (n=3).
    Rabbit Anti Rat Txnip, supplied by Abcam, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti rat txnip/product/Abcam
    Average 98 stars, based on 1 article reviews
    rabbit anti rat txnip - by Bioz Stars, 2026-03
    98/100 stars
    		  Buy from Supplier

    Image Search Results


    The expression of TNXIP in the lesioned spinal cord following compression was observed. ( A ) The TNXIP/NeuN expression in the anterior horn of lesioned spinal cords was analyzed by immunofluorescence. The mean fluorescence intensities of TXNIP were analyzed by Image J software, and represented as mean gray values. ( B ) The TXNIP expression in the lesioned spinal cords was analyzed by Western blot. The gray values of protein bands were analyzed by Image J software, and protein expression was normalized to GAPDH. *P<0.05, **P<0.01.

    Journal: Journal of Inflammation Research

    Article Title: TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy

    doi: 10.2147/JIR.S373614

    Figure Lengend Snippet: The expression of TNXIP in the lesioned spinal cord following compression was observed. ( A ) The TNXIP/NeuN expression in the anterior horn of lesioned spinal cords was analyzed by immunofluorescence. The mean fluorescence intensities of TXNIP were analyzed by Image J software, and represented as mean gray values. ( B ) The TXNIP expression in the lesioned spinal cords was analyzed by Western blot. The gray values of protein bands were analyzed by Image J software, and protein expression was normalized to GAPDH. *P<0.05, **P<0.01.

    Article Snippet: The primary antibodies included rabbit anti-rat TXNIP (1:800, MA5-32771, ThermoFisher), NLRP3 (1:800, MA5-32255, ThermoFisher), pro-caspase-1 (1:800, MA5-35833, ThermoFisher) and GAPDH (1:10000, PA1-16777, ThermoFisher).

    Techniques: Expressing, Immunofluorescence, Fluorescence, Software, Western Blot

    Inhibition of TXNIP improved CSM-induced behavioral deficits. ( A ) The21-point Basso, Beattie and Bresnahan (BBB) locomotor rating scale; ( B ) cold allodynia; ( C ) inclined plane test. Compared with the sham group, **P<0.01; compared with the scrambled group, # P<0.05, ## P<0.01.

    Journal: Journal of Inflammation Research

    Article Title: TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy

    doi: 10.2147/JIR.S373614

    Figure Lengend Snippet: Inhibition of TXNIP improved CSM-induced behavioral deficits. ( A ) The21-point Basso, Beattie and Bresnahan (BBB) locomotor rating scale; ( B ) cold allodynia; ( C ) inclined plane test. Compared with the sham group, **P<0.01; compared with the scrambled group, # P<0.05, ## P<0.01.

    Article Snippet: The primary antibodies included rabbit anti-rat TXNIP (1:800, MA5-32771, ThermoFisher), NLRP3 (1:800, MA5-32255, ThermoFisher), pro-caspase-1 (1:800, MA5-35833, ThermoFisher) and GAPDH (1:10000, PA1-16777, ThermoFisher).

    Techniques: Inhibition

    Inhibition of TXNIP reduced apoptosis in the anterior horn of the lesioned area following CSM. ( A ) Positive TUNEL staining control. ( B ) Apoptosis in the anterior horn of the lesioned area was analyzed by TUNEL staining. Black arrows show apoptotic cells. Apoptosis rate (%) = the numbers of apoptosis cells/total numbers of cells ×100%. The numbers of cells were counted using Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Journal: Journal of Inflammation Research

    Article Title: TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy

    doi: 10.2147/JIR.S373614

    Figure Lengend Snippet: Inhibition of TXNIP reduced apoptosis in the anterior horn of the lesioned area following CSM. ( A ) Positive TUNEL staining control. ( B ) Apoptosis in the anterior horn of the lesioned area was analyzed by TUNEL staining. Black arrows show apoptotic cells. Apoptosis rate (%) = the numbers of apoptosis cells/total numbers of cells ×100%. The numbers of cells were counted using Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Article Snippet: The primary antibodies included rabbit anti-rat TXNIP (1:800, MA5-32771, ThermoFisher), NLRP3 (1:800, MA5-32255, ThermoFisher), pro-caspase-1 (1:800, MA5-35833, ThermoFisher) and GAPDH (1:10000, PA1-16777, ThermoFisher).

    Techniques: Inhibition, TUNEL Assay, Staining, Control, Software

    Inhibition of TXNIP declined the TXNIP expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of TXNIP/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed using Image J software. Compared with the sham group, *P<0.05, **P<0.01; compared with the scrambled group, ## P<0.01.

    Journal: Journal of Inflammation Research

    Article Title: TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy

    doi: 10.2147/JIR.S373614

    Figure Lengend Snippet: Inhibition of TXNIP declined the TXNIP expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of TXNIP/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed using Image J software. Compared with the sham group, *P<0.05, **P<0.01; compared with the scrambled group, ## P<0.01.

    Article Snippet: The primary antibodies included rabbit anti-rat TXNIP (1:800, MA5-32771, ThermoFisher), NLRP3 (1:800, MA5-32255, ThermoFisher), pro-caspase-1 (1:800, MA5-35833, ThermoFisher) and GAPDH (1:10000, PA1-16777, ThermoFisher).

    Techniques: Inhibition, Expressing, Fluorescence, Immunofluorescence, Software

    Inhibition of TXNIP declined the NLRP3 expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of NLRP3/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed by Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Journal: Journal of Inflammation Research

    Article Title: TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy

    doi: 10.2147/JIR.S373614

    Figure Lengend Snippet: Inhibition of TXNIP declined the NLRP3 expression in the anterior horn of the lesioned area following CSM. The mean fluorescence intensities of NLRP3/NeuN were analyzed by immunofluorescence. The mean gray values were analyzed by Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Article Snippet: The primary antibodies included rabbit anti-rat TXNIP (1:800, MA5-32771, ThermoFisher), NLRP3 (1:800, MA5-32255, ThermoFisher), pro-caspase-1 (1:800, MA5-35833, ThermoFisher) and GAPDH (1:10000, PA1-16777, ThermoFisher).

    Techniques: Inhibition, Expressing, Fluorescence, Immunofluorescence, Software

    Inhibition TXNIP declined the NLRP3 mediated pro-caspase-1 expression in the anterior horn of the lesioned area following CSM. ( A ) The mean fluorescence intensities of pro-caspase-1/NeuN were analyzed by immunofluorescence. ( B ) The expression levels of TXNIP, NLRP3 and pro-caspase-1 in the lesioned spinal cords were measured by Western blot. The mean grays were analyzed by the Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Journal: Journal of Inflammation Research

    Article Title: TXNIP Participated in NLRP3-Mediated Inflammation in a Rat Model of Cervical Spondylotic Myelopathy

    doi: 10.2147/JIR.S373614

    Figure Lengend Snippet: Inhibition TXNIP declined the NLRP3 mediated pro-caspase-1 expression in the anterior horn of the lesioned area following CSM. ( A ) The mean fluorescence intensities of pro-caspase-1/NeuN were analyzed by immunofluorescence. ( B ) The expression levels of TXNIP, NLRP3 and pro-caspase-1 in the lesioned spinal cords were measured by Western blot. The mean grays were analyzed by the Image J software. Compared with the sham group, **P<0.01; compared with the scrambled group, ## P<0.01.

    Article Snippet: The primary antibodies included rabbit anti-rat TXNIP (1:800, MA5-32771, ThermoFisher), NLRP3 (1:800, MA5-32255, ThermoFisher), pro-caspase-1 (1:800, MA5-35833, ThermoFisher) and GAPDH (1:10000, PA1-16777, ThermoFisher).

    Techniques: Inhibition, Expressing, Fluorescence, Immunofluorescence, Western Blot, Software

    The impact of ROS and NLRP3 inflammasome on the expression of pyroptosis associated gene and protein. (A)The gene and protein expression of TXNIP, NLRP3, and Caspae-1 in NRK-52E cells under 200 μg/ml uric acid stimulation or not for 24 hr detected by Real-time PCR and western blot techniques (n=3). The cells were categorized into four groups: the control group (0 μg/ml uric acid), the UA group (200 μg/ml uric), the UA+ROS (−) group (200 μg/ml uric + the ROS inhibitors NAC), as well as the UA+mtROS (−) group (200 μg/ml uric+ mtROS inhibitors mt-TEMPO). Data were expressed as mean ± SD. Compared with the UA group, ** P < 0.0001, * P < 0.05. Compared with the UA+ROS (−) group, ⋆⋆ P < 0.0001, ⋆ P < 0.05. Compared with UA+mtROS(−) group, # # P < 0.0001, # P < 0.05.(B) The pyroptosis percent in NRK-52E cells subjected to 200 μg/ml uric acid or not for 24 hr via flow cytometry method (n=3). The cells were divided into four groups: the control group (0 μg/ml uric acid), the UA group (200 μg/ml uric), the UA+NLRP3 (−) group (200 μg/ml uric + the NLRP3 inhibitors MCC950), the UA+Caspase-1(−) group (200 μg/ml uric+ Caspase-1 inhibitors Z-YVAD-FMK). Data were expressed as mean ± SD. Compared with the UA group, ** P < 0.0001, * P < 0.05. Compared with the UA+NLRP3 (-) group, ⋆⋆ P < 0.0001, ⋆ P < 0.05. Compared with UA+Caspase-1(−) group, ## P < 0.0001, # P < 0.05.(C) The gene and protein expression of NLRP3, ASC, Caspae-1, Activated-Caspase-1, GSDMD, IL-1β, and IL-18 in NRK-52E cells when exposed to 200 μg/ml uric acid or not for 24 hr using Real-time PCR and western blot method (n=3).

    Journal: bioRxiv

    Article Title: Hyperuricemia triggers Renal Tubular Epithelial Pyroptosis by using ROS to activate the NLRP3 inflammasome

    doi: 10.1101/2022.03.12.484115

    Figure Lengend Snippet: The impact of ROS and NLRP3 inflammasome on the expression of pyroptosis associated gene and protein. (A)The gene and protein expression of TXNIP, NLRP3, and Caspae-1 in NRK-52E cells under 200 μg/ml uric acid stimulation or not for 24 hr detected by Real-time PCR and western blot techniques (n=3). The cells were categorized into four groups: the control group (0 μg/ml uric acid), the UA group (200 μg/ml uric), the UA+ROS (−) group (200 μg/ml uric + the ROS inhibitors NAC), as well as the UA+mtROS (−) group (200 μg/ml uric+ mtROS inhibitors mt-TEMPO). Data were expressed as mean ± SD. Compared with the UA group, ** P < 0.0001, * P < 0.05. Compared with the UA+ROS (−) group, ⋆⋆ P < 0.0001, ⋆ P < 0.05. Compared with UA+mtROS(−) group, # # P < 0.0001, # P < 0.05.(B) The pyroptosis percent in NRK-52E cells subjected to 200 μg/ml uric acid or not for 24 hr via flow cytometry method (n=3). The cells were divided into four groups: the control group (0 μg/ml uric acid), the UA group (200 μg/ml uric), the UA+NLRP3 (−) group (200 μg/ml uric + the NLRP3 inhibitors MCC950), the UA+Caspase-1(−) group (200 μg/ml uric+ Caspase-1 inhibitors Z-YVAD-FMK). Data were expressed as mean ± SD. Compared with the UA group, ** P < 0.0001, * P < 0.05. Compared with the UA+NLRP3 (-) group, ⋆⋆ P < 0.0001, ⋆ P < 0.05. Compared with UA+Caspase-1(−) group, ## P < 0.0001, # P < 0.05.(C) The gene and protein expression of NLRP3, ASC, Caspae-1, Activated-Caspase-1, GSDMD, IL-1β, and IL-18 in NRK-52E cells when exposed to 200 μg/ml uric acid or not for 24 hr using Real-time PCR and western blot method (n=3).

    Article Snippet: Rabbit anti-rat TXNIP (ab188865), Caspase-1(ab108362), IL-18(ab191860), IL-1β (ab9722) , Caspase-1 p10 (ab179515) antibody were purchased from Abcam (Britain).

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot, Flow Cytometry