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Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
Roche - Proteinase K,recomb.,PCR Grd.Sol.,1.25ml; Solution from Pichia pastoris; pkg of 1.25mL (03115887001) pkg of 25 mL (03115844001) pkg of 5 mL (03115828001)
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A restriction endonuclease that recognizes the sequence ^CCD. Nt.CviPII is a nicking endonuclease that cleaves only one strand of DNA on a double-stranded DNA substrate. The final product on pUC19 is an array of bands from 25 to 200 bp. CCT is cut less efficiently than CCG and CCA. Some of the CCT sites are not cleaved. (Based on NEB observations.)
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T7 Endonuclease I (T7E1) recognizes and cleaves non-perfectly matched DNA cruciform DNA structures Holliday structures or junctions hetero duplex DNA and more slowly nicked double-stranded DNA The cleavage site is at the first second or third phosphodiester bond that is 5 to the mismatch The protein is the product of T7 gene 3 GenCrispr T7 Endonuclease I is a fusion protein produced from i E coli /i
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Aquaphile coelenterazine native is a bioluminescence substrate in a special formulation format that is readily dissolved in water or PBS buffer for in vivo use.Properties: Yellow solid soluble in water or PBS buffer; Store at -20°C and protect from light; C26H21N3O3; MW: 423; [55779-48-1].
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The SGKtide peptide sequence (CKKRNRRLSVA) contains serine protein kinase phosphorylation site and is evaluated as a substrate for SGK and NDR family kinases.
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TtAgo is a prokaryotic argonaute from the Gram-negative, thermophilic bacterium Thermus thermophilus which functions as a DNA-guided endonuclease when provided with a 16-18 nucleotide long 5-phosphorylated single-stranded DNA oligonucleotide guide. The RNase H-like active site of TtAgo requires divalent Mg2+ (or Mn2+) metal ions for the reaction to occur and cleaves a complementary substrate between the bases corresponding to positions 10 and 11 of the DNA guide.
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