shRNA gene silencing Human TF‐1

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Get tips on using Endothelin-1 Quantikine ELISA Kit to perform ELISA Rat - Endothelin 1

Products R&D Systems Endothelin-1 Quantikine ELISA Kit

Get tips on using Endothelin 1 ELISA Kit (ab133030) to perform ELISA Rat - Endothelin 1

Products Abcam Endothelin 1 ELISA Kit (ab133030)

Get tips on using Beclin-1 Antibody to perform Autophagy assay cell type - NRK-49F

Products Cell Signaling Technology Beclin-1 Antibody

Get tips on using Beclin-1 Antibody to perform Autophagy assay cell type - BRL-3A

Products Cell Signaling Technology Beclin-1 Antibody

Get tips on using pLKO.1 puro to perform CRISPR Mouse - Activation RAW 264.7 Dmd

Products Addgene pLKO.1 puro

Get tips on using pLKO.1 puro to perform CRISPR Mouse - Deletion 3T3-L1 Epac1

Products Addgene pLKO.1 puro
pGEX-4T-1 Product

Get tips on using pGEX-4T-1 to perform Protein Expression Prokaryotic cells - E. coli LsrK

Products Kyoung-Seok Ryu, Protein Structure Group, Korea Basic Science In pGEX-4T-1

DNA-protein interactions are studied by using ChIP. The basic steps in this technique are crosslinking, sonication, immunoprecipitation, and analysis of the immunoprecipitated DNA. During ChIP, if chromatin is under-fragmented or fragments are too large which can lead to the increased background and lower resolution. Shorter cross-linking times (5-10 min) and/or lower formaldehyde concentrations (<1%) may improve shearing efficiency. If Chromatin is over-fragmented, then optimize shearing conditions for each cell type to improve ChIP efficiency. Over-sonication of chromatin may disrupt chromatin integrity and denature antibody epitopes. If you do not see any product or very little product in the input PCR reactions, add 5–10 μg chromatin per IP.

Proteins ChIP Mouse Hepa-1

DNA-protein interactions are studied by using ChIP. The basic steps in this technique are crosslinking, sonication, immunoprecipitation, and analysis of the immunoprecipitated DNA. During ChIP, if chromatin is under-fragmented or fragments are too large which can lead to the increased background and lower resolution. Shorter cross-linking times (5-10 min) and/or lower formaldehyde concentrations (<1%) may improve shearing efficiency. If Chromatin is over-fragmented, then optimize shearing conditions for each cell type to improve ChIP efficiency. Over-sonication of chromatin may disrupt chromatin integrity and denature antibody epitopes. If you do not see any product or very little product in the input PCR reactions, add 5–10 μg chromatin per IP.

Proteins ChIP Rat INS-1

Get tips on using Beclin-1 (D40C5) Rabbit mAb to perform Autophagy assay cell type - THP 1

Products Cell Signaling Technology Beclin-1 (D40C5) Rabbit mAb

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