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GenScript corporation shelterin genes (terf1, terf2, terf2ip/rap1, tinf2, acd/tpp1, pot1
a. Outline of DNaseI footprinting experiment. 32 P-labelled 5’ end highlighted by a red asterisk. Radiolabelled template is incubated with KU and DNAPKcs prior to the addition of <t>Shelterin</t> composed of TRF1, <t>TRF2,</t> <t>RAP1,</t> TIN2, <t>POT1</t> and <t>TPP1.</t> DNase I digested products are then analysed by denaturing Urea-PAGE b-f. DNaseI footprinting of telomere end-binding complexes. Proteins omitted as indicated. Nucleotides from the 5’ telomeric end indicated.
Shelterin Genes (Terf1, Terf2, Terf2ip/Rap1, Tinf2, Acd/Tpp1, Pot1, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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a. Outline of DNaseI footprinting experiment. 32 P-labelled 5’ end highlighted by a red asterisk. Radiolabelled template is incubated with KU and DNAPKcs prior to the addition of Shelterin composed of TRF1, TRF2, RAP1, TIN2, POT1 and TPP1. DNase I digested products are then analysed by denaturing Urea-PAGE b-f. DNaseI footprinting of telomere end-binding complexes. Proteins omitted as indicated. Nucleotides from the 5’ telomeric end indicated.

Journal: bioRxiv

Article Title: Chromosome end protection by RAP1-mediated inhibition of DNA-PK

doi: 10.1101/2024.12.28.630583

Figure Lengend Snippet: a. Outline of DNaseI footprinting experiment. 32 P-labelled 5’ end highlighted by a red asterisk. Radiolabelled template is incubated with KU and DNAPKcs prior to the addition of Shelterin composed of TRF1, TRF2, RAP1, TIN2, POT1 and TPP1. DNase I digested products are then analysed by denaturing Urea-PAGE b-f. DNaseI footprinting of telomere end-binding complexes. Proteins omitted as indicated. Nucleotides from the 5’ telomeric end indicated.

Article Snippet: The shelterin genes (TERF1, TERF2, TERF2IP/RAP1, TINF2, ACD/TPP1, POT1), codon-optimised for E. coli , were synthesised by GenScript and cloned into pACEBAC1, using a nicking cloning system .

Techniques: Footprinting, Incubation, Binding Assay