Capillary array electrophoresis (CAE) chips have been designed and fabricated with the capacity to rapidly (< 160 s) analyze 12 different samples in parallel, Detection of all lanes with 0.3 s temporal resolution was achieved using a laser-excited confocal-fluorescence scanner. The operation and capabilities of these CAE microdevices were first determined by performing electrophoretic separations of pBR322 MspI DNA samples. Genotyping of HLA-H, a candidate gene for the diagnosis of hereditary hemochromatosis, was then performed to demonstrate the rapid analysis of biologically relevant samples. Two-color multiplex fluorescence detection of HIA-H genotypes was accomplished by prelabeling the standard pBR322 MspI DNA ladder with a red emitting bisintercalation dye (butyl TOTIN) and on-column labeling of the HLA-H DNA with thiazole orange. This work establishes the feasibility of using CAE chips for highspeed, high-throughput genotyping.
机构:
UNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USAUNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USA
SWERDLOW, H
GESTELAND, R
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机构:
UNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USAUNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USA
机构:
UNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USAUNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USA
SWERDLOW, H
GESTELAND, R
论文数: 0引用数: 0
h-index: 0
机构:
UNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USAUNIV UTAH, HOWARD HUGHES MED INST, DEPT BIOENGN, SALT LAKE CITY, UT 84132 USA