rna-isolation-purification-cells-immortalized-mda-mb-361

- Found 9121 results

Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - Paneth cells

Products Sigma-Aldrich Anti-LC3B antibody produced in rabbit

Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - Goblet cells

Products Sigma-Aldrich Anti-LC3B antibody produced in rabbit

Get tips on using Anti-LC3B antibody produced in rabbit to perform Autophagy assay cell type - K562 cells

Products Sigma-Aldrich Anti-LC3B antibody produced in rabbit

Get tips on using CellTiter-Glo® Luminescent Cell Viability Assay to perform Live / Dead assay mammalian cells - BHK-21

Products Promega CellTiter-Glo® Luminescent Cell Viability Assay

Get tips on using siGENOME Rat Nrp1 siRNA to perform siRNA / miRNA gene silencing Rat - Schwann cells Nrp1

Products Dharmacon siGENOME Rat Nrp1 siRNA

Get tips on using LC3A/B (D3U4C) XP® Rabbit mAb #12741 to perform Autophagy assay cell type - HK-2 cells

Products Cell Signaling Technology LC3A/B (D3U4C) XP® Rabbit mAb #12741

Get tips on using LC3A/B (D3U4C) XP® Rabbit mAb #12741 to perform Autophagy assay cell type - HK-2 cells

Products Cell Signaling Technology LC3A/B (D3U4C) XP® Rabbit mAb #12741

Get tips on using LC3A/B (D3U4C) XP® Rabbit mAb #12741 to perform Autophagy assay cell type - HK-2 cells

Products Cell Signaling Technology LC3A/B (D3U4C) XP® Rabbit mAb #12741

A restriction enzyme or restriction endonuclease is defined as a protein that recognizes a specific, short nucleotide sequence and cuts the DNA only at or near that site, known as restriction site or target sequence. The four most common types of restriction enzymes include: Type I (cleaves at sites remote from a recognition site), Type II (cleaves within or at short specific distances from a recognition site), Type III (cleave at sites a short distance from a recognition site), and Type IV (targets modified DNA- methylated, hydroxymethylated and glucosyl-hydroxymethylated DNA). The most common challenges with restriction digest include- 1. inactivation of the enzyme, 2. incomplete or no digestion, and 3. unexpected cleavage. The enzyme should always be stored at -20C and multiple freeze-thaw cycles should be avoided in order to maintain optimal activity. Always use a control DNA digestion with the enzyme to ensure adequate activity (to avoid interference due to high glycerol in the enzyme). For complete digestion, make sure that the enzyme volume is 1/10th of the total reaction volume, the optimal temperature is constantly maintained throughout the reaction, the total reaction time is appropriately calculated based on the amount of DNA to be digested, appropriate buffers should be used to ensure maximal enzymatic activity, and in case of a double digest, make sure that the two restriction sites are far enough so that the activity of one enzyme cannot interfere with the activity of the other. Star activity (or off-target cleavage) and incomplete cleavage are potential challenges which may occur due to suboptimal enzymatic conditions or inappropriate enzyme storage. To avoid these, follow the recommended guidelines for storage and reactions, and always check for the efficacy of digestion along with purification of digested products on an agarose gel.

Proteins Restriction Enzymes BstNI / MvaI

Get tips on using RealTime-Glo™ MT Cell Viability Assay to perform Live / Dead assay mammalian cells - INS-1 832/12

Products Promega RealTime-Glo™ MT Cell Viability Assay

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