siRNA / miRNA gene silencing Human HeLa EPAS-1

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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 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
mTeSR™1 Product

Get tips on using mTeSR™1 to perform Stem cell culture media hESC lines H9, H1

Products STEMCELL technologies mTeSR™1

Get tips on using CD133 (Prominin-1) Monoclonal Antibody (13A4), APC, eBioscience™ to perform Flow cytometry Anti-bodies Human - CD133

Products eBioscience CD133 (Prominin-1) Monoclonal Antibody (13A4), APC, eBioscience™

Get tips on using Human ICAM1 ELISA Kit (CD54) (ab100640) to perform ELISA Human - ICAM-1/CD54

Products Abcam Human ICAM1 ELISA Kit (CD54) (ab100640)
pPG-1-FlaA Product

Get tips on using pPG-1-FlaA to perform Protein Expression Prokaryotic cells - E. coli surface flagellin A

Products Gui-Qin Wang, College of Animal Science and Technology, Jilin Ag pPG-1-FlaA

Get tips on using pET-21b(+)/Pro j 1 to perform Protein Expression Prokaryotic cells - E. coli Pro J 1

Products Mohammad-Ali Assarehzadegan, Department of Immunology, Faculty o pET-21b(+)/Pro j 1

A key signature for necrotic cells is the permeabilization of the plasma membrane. Necrosis can be quantified by several cellular and biochemical assays. When studied minutely, it reveals the difficulty in confirmation in secondary induction of necrosis in apoptotic cells. Apoptotic cells are being analyzed to shift to necrotic status owing to membrane permeability at later stages, and thus, discrimination of two cell death becomes critical. Therefore, it is crucial to use a necrosis detection kit or a defined procedure to analyze this unprogrammed form of death in response to immense chemical and physical insults.

Cellular assays Necrosis PANC-1

Get tips on using GDNF RECEPTOR ALPHA 1 to perform Immunohistochemistry Mouse - GFRA1

Products Neuromics GDNF RECEPTOR ALPHA 1

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