The largest database of trusted experimental protocols

2 protocols using anti chga

1

Comprehensive Antibody Characterization Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
The primary antibodies used in this study were as follows: anti-BRG1 (EPNCIR111A) Abcam Cat# ab110641 (1:10,000); anti-Caspase3 (8G10), Cell Signaling Technology, Cat# 9665 (1:1000); anti-C-Caspase 3, Cell Signaling Technology, Cat# 9661 (1:1000); anti-PARP (46D11), Cell Signaling Technology, Cat# 9532 (1:1000); anti-Ki67 (B56), BD Biosciences, Cat# 550609 (1:500); anti-EpCAM (G8.8), BD Biosciences, Cat# 552370 (1:500); anti-ZO1, Invitrogen, Cat# 40-2200 (1:500); anti-8-OHd G, Abcam, Cat# ab48508 (1:500); anti-LC3A/B (D3U4C), Cell Signaling Technology, Cat# 12741 (1:1000); anti-ATG16L1 (D6A5), Cell Signaling Technology, Cat# 8089 (1:1000); anti-PCNA, Santa Cruz Biotechnology, Cat# SC-7909 (1:1000); anti-P-H3, Cell Signaling Technology, Cat# 9701 (1:1000); anti-E-Cadherin, Cell Signaling Technology, Cat# 3195T (1:1000); anti-DCLK1, Abcam, Cat# ab31704 (1:500); anti-Claudin1, Cell Signaling Technology, Cat# 4933T (1:1000); anti-ChgA, Abcam, Cat# ab715 (1:1000); anti-Hes1, Abcam, Cat# ab71559 (1:500). Raw data of immunoblotting can be found in the source data file.
+ Open protocol
+ Expand
2

Intestinal Goblet and Enteroendocrine Cell Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Mouse colon was fixed in 10% neutral formalin and stored in 70% ethanol. Intestinal samples were then paraffin-embedded and cut into 10 um longitudinal sections, and the PAS staining was performed by Histoserv Inc. (Germantown, MD). Goblet cells were counted and calculated from 10 crypts in each slide.
For immunofluorescence staining, slides were deparaffinized by xylene and antigen retrieval was conducted for 20 min in a 95°-water bath in 10 mM sodium citrate, pH 6.0 followed by a 15 min incubation at room temperature. Slides were washed, blocked in 5% bovine serum albumin, and stained with the primary antibodies, anti-ChgA (1:100; Abcam), anti-5-HT (1:100; Abcam), anti-ST2 (1:100, Proteintech) and anti-TRPA1 (1:100, Novus) and secondary antibodies conjugated to Alexa fluor 488, 633 or 594 (Thermo Fisher). Slides were mounted in Fluoromount-G (Thermo Fisher), and 3–15 images were taken per slide at 20X or 40X magnification along transections of the intestinal crypts for each biological replicate (Zeiss). For 5-HT and ChgA staining, numbers of positively stained puncta were scored blindly, normalized to total area of intestinal mucosa using ImageJ software (NIH), and then averaged across biological replicates.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!