Chromatin accessibility assay

RU Rocio G Urdinguio
VL Virginia Lopez
GB Gustavo F Bayón
RD Rafael Diaz de la Guardia
MS Marta I Sierra
EG Estela García-Toraño
RP Raúl F Perez
MG María G García
AC Antonella Carella
PP Patricia C Pruneda
CP Cristina Prieto
MD Marija Dmitrijeva
PS Pablo Santamarina
TB Thalía Belmonte
CM Cristina Mangas
ED Elena Diaconu
CF Cecilia Ferrero
JT Juan Ramón Tejedor
JF Juan Luis Fernandez-Morera
CB Cristina Bravo
CB Clara Bueno
AS Alejandra Sanjuan-Pla
RR Ramon M Rodriguez
BS Beatriz Suarez-Alvarez
CL Carlos López-Larrea
TB Teresa Bernal
EC Enrique Colado
MB Milagros Balbín
OG Olivia García-Suarez
MC María Dolores Chiara
IS Inés Sáenz-de-Santa-María
FR Francisco Rodríguez
AP Ana Pando-Sandoval
LR Luis Rodrigo
LS Laura Santos
AS Ana Salas
JV Jesús Vallejo-Díaz
AC Ana C. Carrera
DR Daniel Rico
IH Inmaculada Hernández-López
AV Amparo Vayá
JR José M Ricart
ES Edward Seto
NS Núria Sima-Teruel
AV Alejandro Vaquero
LV Luis Valledor
MC Maria Jesus Cañal
DP David Pisano
OG Osvaldo Graña-Castro
TT Tim Thomas
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For the analysis of chromatin accessibility in multiple repetitive elements, 1 × 106 CD15+ CD16+ neutrophils and 1 × 106 CD3+ lymphocytes from four donors were subjected to chromatin extraction and nuclease digestion according to manufacturer's instructions (EpiQuik Chromatin Accessibility Assay kit, P-1047 Epigentek). Purified DNA was analyzed via real time qPCR using primers for different repeats (see Supplementary Table S1). Fold enrichment (FE) was calculated as the ratio of amplification efficiency (Ct) of the digested DNA sample over that of the non-digested sample. Large Ct shifts between digested and undigested samples, rendering high FE%, indicated that the target region was in the open chromatin, while minimal Ct shifts, resulting in low FE%, indicated that the target region was in the closed chromatin.

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