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triple roll mill exakt 80e  (EXAKT Technologies)
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symphony x  (Gyros Protein Technologies)
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als cst  (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc als cst
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hrp  (Cell Signaling Technology Inc)
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rabbit anti psd95  (Cell Signaling Technology Inc)
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phosho 44 22 mapk thr202 tyr204  (Cell Signaling Technology Inc)
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cathepsin d e179 rabbit antibody  (Cell Signaling Technology Inc)
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wdr77  (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc wdr77
Fig. 4. A set of 15 genes change in opposite directions at the mRNA level in denervation and obstruction. The Venny analysis tool was used to identify genes that were increased in denervation (at Q 0.05) and reduced in obstruction (at Q 0.05) or vice versa. Fifteen mRNAs satisfied these criteria. Changes of these mRNAs are plotted in A–C. Italicized gene products met the Q 0 criterion, and the remainder met the Q 0.05 criterion. D: 4 examples of immunohistochemical stainings from the Human Protein Atlas for gene products in this set. Brown indicates positive staining. Antibodies for all of these targets stained the urothelial cell layer of the bladder. E: Western blots for <t>Wdr77</t> and Flot2 in denervation and obstruction.
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ifn ribavirin therapy  (Cell Signaling Technology Inc)
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Fig. 4. A set of 15 genes change in opposite directions at the mRNA level in denervation and obstruction. The Venny analysis tool was used to identify genes that were increased in denervation (at Q 0.05) and reduced in obstruction (at Q 0.05) or vice versa. Fifteen mRNAs satisfied these criteria. Changes of these mRNAs are plotted in A–C. Italicized gene products met the Q 0 criterion, and the remainder met the Q 0.05 criterion. D: 4 examples of immunohistochemical stainings from the Human Protein Atlas for gene products in this set. Brown indicates positive staining. Antibodies for all of these targets stained the urothelial cell layer of the bladder. E: Western blots for <t>Wdr77</t> and Flot2 in denervation and obstruction.
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antibody b catenin cat 9587s cell signaling  (Cell Signaling Technology Inc)
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Fig. 4. A set of 15 genes change in opposite directions at the mRNA level in denervation and obstruction. The Venny analysis tool was used to identify genes that were increased in denervation (at Q 0.05) and reduced in obstruction (at Q 0.05) or vice versa. Fifteen mRNAs satisfied these criteria. Changes of these mRNAs are plotted in A–C. Italicized gene products met the Q 0 criterion, and the remainder met the Q 0.05 criterion. D: 4 examples of immunohistochemical stainings from the Human Protein Atlas for gene products in this set. Brown indicates positive staining. Antibodies for all of these targets stained the urothelial cell layer of the bladder. E: Western blots for <t>Wdr77</t> and Flot2 in denervation and obstruction.
Antibody B Catenin Cat 9587s Cell Signaling, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse anti human pp65  (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc mouse anti human pp65
Fig. 4. A set of 15 genes change in opposite directions at the mRNA level in denervation and obstruction. The Venny analysis tool was used to identify genes that were increased in denervation (at Q 0.05) and reduced in obstruction (at Q 0.05) or vice versa. Fifteen mRNAs satisfied these criteria. Changes of these mRNAs are plotted in A–C. Italicized gene products met the Q 0 criterion, and the remainder met the Q 0.05 criterion. D: 4 examples of immunohistochemical stainings from the Human Protein Atlas for gene products in this set. Brown indicates positive staining. Antibodies for all of these targets stained the urothelial cell layer of the bladder. E: Western blots for <t>Wdr77</t> and Flot2 in denervation and obstruction.
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Image Search Results


Journal: iScience

Article Title: A purinergic mechanism underlying metformin regulation of hyperglycemia

doi: 10.1016/j.isci.2023.106898

Figure Lengend Snippet:

Article Snippet: Rabbit anti-mouse lgG (light chain specific) secondary antibody, HRP , Cell Signaling , #58802.

Techniques: Virus, Recombinant, SYBR Green Assay, Calcium Mobilization Assay, ATP Assay, Glucose Assay, Detection Assay, Control, Software, Plasmid Preparation, Inverted Microscopy

Fig. 4. A set of 15 genes change in opposite directions at the mRNA level in denervation and obstruction. The Venny analysis tool was used to identify genes that were increased in denervation (at Q 0.05) and reduced in obstruction (at Q 0.05) or vice versa. Fifteen mRNAs satisfied these criteria. Changes of these mRNAs are plotted in A–C. Italicized gene products met the Q 0 criterion, and the remainder met the Q 0.05 criterion. D: 4 examples of immunohistochemical stainings from the Human Protein Atlas for gene products in this set. Brown indicates positive staining. Antibodies for all of these targets stained the urothelial cell layer of the bladder. E: Western blots for Wdr77 and Flot2 in denervation and obstruction.

Journal: American journal of physiology. Renal physiology

Article Title: Array profiling reveals contribution of Cthrc1 to growth of the denervated rat urinary bladder.

doi: 10.1152/ajprenal.00499.2017

Figure Lengend Snippet: Fig. 4. A set of 15 genes change in opposite directions at the mRNA level in denervation and obstruction. The Venny analysis tool was used to identify genes that were increased in denervation (at Q 0.05) and reduced in obstruction (at Q 0.05) or vice versa. Fifteen mRNAs satisfied these criteria. Changes of these mRNAs are plotted in A–C. Italicized gene products met the Q 0 criterion, and the remainder met the Q 0.05 criterion. D: 4 examples of immunohistochemical stainings from the Human Protein Atlas for gene products in this set. Brown indicates positive staining. Antibodies for all of these targets stained the urothelial cell layer of the bladder. E: Western blots for Wdr77 and Flot2 in denervation and obstruction.

Article Snippet: Following one-dimensional (1D) separation and transfer to nitrocellulose, proteins were detected using the following antibodies: CTHRC1 (mmcri, vli55), PRC1 (no. 3639; Cell Signaling), PLOD2 (21214–1-AP; Proteintech), DKK3 (ab186409; Abcam), PERK (no. 3192; Cell Signaling), CAV1 (no. 3267; Cell Signaling), myosin phosphatase targeting subunit (MYPT/MYPT1, no. 2634; Cell Signaling), myosin light chain kinase (MYLK, M 7905; Sigma), pleiotrophin (PTN, ab79411; Abcam), gelsolin (GSN, no. 12953; Cell Signaling), osteopontin (SPP1, ab91665; Abcam), CD68 (MCA5709; Bio-Rad), WDR77 (D56B8, no. 2018S; Cell Signaling), FLOT2 (no. 3436S; Cell Signaling), -actin (A5441; Sigma Aldrich), and HSP90 (610418; BD Transduction Laboratories).

Techniques: Immunohistochemical staining, Staining, Western Blot