Immunohistochemistry Alpha smooth muscle Actin Mouse -NA-

- Found 2875 results

pX330A-1x3 Product

Get tips on using pX330A-1x3 to perform CRISPR Mouse - Deletion ATDC5 Perk

Products Addgene pX330A-1x3

Get tips on using gRNA_Cloning Vector to perform CRISPR Mouse - Deletion L929 Gβ2

Products Addgene gRNA_Cloning Vector

Get tips on using pSpCas9 (PX165) to perform CRISPR Mouse - Deletion C2C12 Klf5

Products Addgene pSpCas9 (PX165)

Get tips on using pSpCas9 (PX165) to perform CRISPR Mouse - Deletion αT3 IP3R1

Products Addgene pSpCas9 (PX165)

Get tips on using TruSeq Stranded mRNA to perform RNA sequencing Mouse - C2C12

Products Illumina TruSeq Stranded mRNA

Get tips on using ChromaFlash Chromatin Extraction Kit to perform ChIP Mouse - Osteoblasts

Products Epigentek ChromaFlash Chromatin Extraction Kit

Get tips on using EpiTect ChIP OneDay Kit to perform ChIP Mouse - MIN6

Products Qiagen EpiTect ChIP OneDay Kit

Get tips on using EpiTect ChIP qPCR Assays to perform ChIP Mouse - NIH3T3

Products Qiagen EpiTect ChIP qPCR Assays

Get tips on using HSP70 ELISA Kit (ab133060) to perform ELISA Mouse - HSP70

Products Abcam HSP70 ELISA Kit (ab133060)

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 PdiI / NaeI

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