The largest database of trusted experimental protocols

Peroxidase affinipure goat anti rabbit mouse igg h l

Manufactured by Jackson ImmunoResearch
Sourced in United States

Peroxidase-AffiniPure Goat Anti-Rabbit/Mouse IgG (H+L) is a secondary antibody conjugated with the enzyme peroxidase. It is designed to detect and bind to rabbit or mouse immunoglobulin G (IgG) antibodies in a laboratory setting.

Automatically generated - may contain errors

3 protocols using peroxidase affinipure goat anti rabbit mouse igg h l

1

Western Blot Analysis of GCase

Check if the same lab product or an alternative is used in the 5 most similar protocols
Triton (1%) lysis buffer was used to lyse the fibroblast cells after compound treatment, and then 20% SDS sample buffer was used to denature the proteins at 100 °C for 10 min. Bis-Tris gel (10%, Life Tech) was used for running gels and Trans-Blot Turbo PVDF kit (Bio-Rad) was used to transfer membranes. GCase antibody (Sigma-Aldrich) and GAPDH primary antibodies were incubated with the membranes overnight, then the incubated membranes were treated with the secondary antibody (Peroxidase-AffiniPure Goat Anti-Rabbit/Mouse IgG (H+L), Jackson Immunoresearch Lab) for 30 min. Chemidoc MP system (Bio-Rad) was used to scan the membranes and analyze the imaging.
+ Open protocol
+ Expand
2

Western Blot Analysis of GCase Protein

Check if the same lab product or an alternative is used in the 5 most similar protocols
Proteins were denatured in 20% SDS sample buffer at 100 °C for 10 min; 10% Bis-Tris gel (Life Tech) was used for gels; Trans-Blot Turbo PVDF kit (Bio-Rad) was used for membrane transfer. GCase antibody (Sigma-Aldrich) and GAPDH primary antibodies (EMD Millipore) were incubated with the membranes overnight, then the incubated membranes were treated with the secondary antibody (Peroxidase-AffiniPure Goat Anti-Rabbit/Mouse IgG (H+L), Jackson Immunoresearch Lab) for 30 min. Chemidoc MP system (Bio-Rad) was used to scan the membranes and analyze the imaging.
+ Open protocol
+ Expand
3

Western Blot Protein Expression Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Total cellular proteins were extracted using RIPA lysis buffer (Beyotime), separated via electrophoresis on a 10% SDS separation gel (YEASEN, China), and transferred to PVDF membranes (Millipore, Germany). The PVDF membranes were then incubated with primary antibodies, including anti-SRSF5 (1:1000; Abcam, UK), anti-HOXD8 (1:1000; Santa Cruz, USA), anti-TRIM72 (1:2000; Proteintech, USA), anti-PKM2 (1:1000; CST, USA), and anti-GAPDH (1:5000; ABclonal, China) antibodies at 4 °C. Subsequently, the membranes were incubated with Peroxidase AffiniPure Goat Anti-Rabbit/Mouse IgG (H + L) (1:10000; Jackson ImmunoResearch, USA) for 1 h at room temperature. The protein bands were visualized with a SuperPico ECL Chemiluminescence Kit (Vazyme) and imaged using a ChemiDoc XRS + Imaging System (Bio-Rad, USA).
+ 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!