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anti tubulin monoclonal antibody  (Proteintech)
96
Proteintech anti tubulin monoclonal antibody
Anti Tubulin Monoclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti tubulin monoclonal antibody/product/Proteintech
Average 96 stars, based on 1 article reviews
anti tubulin monoclonal antibody - by Bioz Stars, 2026-02
96/100 stars
  Buy from Supplier
tubulin  (Proteintech)
96
Proteintech tubulin
Lap/Hep@FGF4 enhances axon regeneration through microtubule stabilization. (A) Double immunofluorescence staining of <t>Ace-tubulin</t> (green) and NF-200 (red) in axons at the lesion site on the 28th day after SCI. (B, C) Quantification data of Ace-tubulin positive and NF-200 positive area in spinal cord. (D-G) Protein expression and quantification data of Ace-tubulin, Detyr-tubulin and Tyr-tubulin in each group. All experiments were performed in triplicate and values were expressed as the Mean ± SD, n= 4 per group.
Tubulin, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/tubulin/product/Proteintech
Average 96 stars, based on 1 article reviews
tubulin - by Bioz Stars, 2026-02
96/100 stars
  Buy from Supplier

Image Search Results


Lap/Hep@FGF4 enhances axon regeneration through microtubule stabilization. (A) Double immunofluorescence staining of Ace-tubulin (green) and NF-200 (red) in axons at the lesion site on the 28th day after SCI. (B, C) Quantification data of Ace-tubulin positive and NF-200 positive area in spinal cord. (D-G) Protein expression and quantification data of Ace-tubulin, Detyr-tubulin and Tyr-tubulin in each group. All experiments were performed in triplicate and values were expressed as the Mean ± SD, n= 4 per group.

Journal: Theranostics

Article Title: An injectable heparin-Laponite hydrogel bridge FGF4 for spinal cord injury by stabilizing microtubule and improving mitochondrial function

doi: 10.7150/thno.37601

Figure Lengend Snippet: Lap/Hep@FGF4 enhances axon regeneration through microtubule stabilization. (A) Double immunofluorescence staining of Ace-tubulin (green) and NF-200 (red) in axons at the lesion site on the 28th day after SCI. (B, C) Quantification data of Ace-tubulin positive and NF-200 positive area in spinal cord. (D-G) Protein expression and quantification data of Ace-tubulin, Detyr-tubulin and Tyr-tubulin in each group. All experiments were performed in triplicate and values were expressed as the Mean ± SD, n= 4 per group.

Article Snippet: After blockade in Tris-buffered saline plus 5% (w/v) milk (Bio-Rad), membranes were exposed to primary antibodies: GFAP (1:2000, Abcam), NF-200 (1:2000, Abcam), microtubule-associated protein 2 (MAP-2, 1:1000, Cell Signaling Technologies), NG-2 (1:1000, Abcam), Laminin (1:1000, Abcam), Neurocan (1:1000, Abcam), MBP (1:1000, Abcam), CD68 (1:1000, Abcam), Ace-tubulin (1:1000, Abcam), Detyrosinated tubulin (1:500, Proteintech, China), Tyrosinated tubulin (1:500, Proteintech, China) and GAPDH (1:1000, Cell Signaling Technologies), in the blocking solution overnight at 4 ° C. Horseradish peroxidase-conjugated rabbit/mouse-specific antibodies were incubated with samples for 60 min at room temperature.

Techniques: Double Immunofluorescence Staining, Expressing

Lap/Hep@FGF4 enhances axon formation via microtubule‐stabilization in neurons. (A) Beta-3 tubulin (Tuj-1) immunolabeling of neurons with or without inhibitory chondroitin sulfate proteoglycans (CSPGs, 3.34 µg/mL) substrates in primary cortical neurons. (B) Co‐immunofluorescence images show Ace‐tubulin (green) and Tyr‐tubulin (red) in primary cortical neurons. (C, D) Quantification of A/T ratio and axonal length from B. (E-H) Protein expression and quantification data of Ace-tubulin, Detyr-tubulin and Tyr-tubulin in each group. All experiments were performed in triplicate and values were expressed as the Mean ± SD.

Journal: Theranostics

Article Title: An injectable heparin-Laponite hydrogel bridge FGF4 for spinal cord injury by stabilizing microtubule and improving mitochondrial function

doi: 10.7150/thno.37601

Figure Lengend Snippet: Lap/Hep@FGF4 enhances axon formation via microtubule‐stabilization in neurons. (A) Beta-3 tubulin (Tuj-1) immunolabeling of neurons with or without inhibitory chondroitin sulfate proteoglycans (CSPGs, 3.34 µg/mL) substrates in primary cortical neurons. (B) Co‐immunofluorescence images show Ace‐tubulin (green) and Tyr‐tubulin (red) in primary cortical neurons. (C, D) Quantification of A/T ratio and axonal length from B. (E-H) Protein expression and quantification data of Ace-tubulin, Detyr-tubulin and Tyr-tubulin in each group. All experiments were performed in triplicate and values were expressed as the Mean ± SD.

Article Snippet: After blockade in Tris-buffered saline plus 5% (w/v) milk (Bio-Rad), membranes were exposed to primary antibodies: GFAP (1:2000, Abcam), NF-200 (1:2000, Abcam), microtubule-associated protein 2 (MAP-2, 1:1000, Cell Signaling Technologies), NG-2 (1:1000, Abcam), Laminin (1:1000, Abcam), Neurocan (1:1000, Abcam), MBP (1:1000, Abcam), CD68 (1:1000, Abcam), Ace-tubulin (1:1000, Abcam), Detyrosinated tubulin (1:500, Proteintech, China), Tyrosinated tubulin (1:500, Proteintech, China) and GAPDH (1:1000, Cell Signaling Technologies), in the blocking solution overnight at 4 ° C. Horseradish peroxidase-conjugated rabbit/mouse-specific antibodies were incubated with samples for 60 min at room temperature.

Techniques: Immunolabeling, Immunofluorescence, Expressing