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Heparin coated capillary tubes

Manufactured by Drummond
Sourced in United States

Heparin-coated capillary tubes are specialized laboratory equipment used for the collection and analysis of blood samples. The capillary tubes are coated with the anticoagulant heparin, which prevents the blood from clotting during the collection and testing processes.

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4 protocols using heparin coated capillary tubes

1

Restraint Stress Induces Corticosterone

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During the animal’s light cycle between 10:00 and 13:00, single-housed mice were restrained for 15 min in modified 50 ml conical tubes with the cone endings removed and an aperture added to the cap for the tail. Tail blood was collected with heparin-coated capillary tubes (Drummond) at time points 0, 15, 30 and 90 min from the onset of restraint stress. Plasma was collected from blood by centrifugation at 2,000× g for 10 min. CORT levels were measured in plasma using CORT ELISA kit (Enzo Life Sciences). Using 5 μL of plasma, samples were prepared and analyzed in duplicate on a 96-well plate following manufacturer’s protocol.
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2

Ethanol Consumption in Mice Drinking in the Dark

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The drinking in the dark assay was performed based on published methods (Thiele et al., 2014 (link)). For four nights, single-housed mice were habituated in the home cage to one 25 ml sipper tube filled with water that replaced their regular water bottle 2 h into the animal’s dark cycle. After the final habituation trial, sipper tubes were filled with 20% (w/vol) ethanol and consumption was measured for 2 h training trials over three consecutive days and for 4 h in a test trial on the final day.
To examine blood ethanol concentrations (BEC) immediately following the test trial, ≤10 μL tail vein blood was collected from each animal using heparin-coated capillary tubes (Cat# 1-000-3200-H; Drummond, Broomall, PA, USA). Tail blood was centrifuged at 2,000× g for 10 min and plasma was stored at −80°C prior to being measured for ethanol (mg/dL) using an AM1 Analox Ethanol analyzer (Analox Instruments, London, UK).
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3

Restraint Stress Response in Mice

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Twelve-week-old male and female E- and C-sired offspring were subjected to a 15-min restraint stress exposure. All animals were tested between 3 and 5 h after lights-on (10:00 AM to 12:00 noon). Briefly, mice were removed from group housing and restrained in conical plastic tubes with several air hole perforations near the animal’s head and an opening for the tail. After the 15-min restraint, each mouse was returned to a single novel cage until the 90-min time point. Only one mouse was tested per group-housed cage to avoid pre-stressing any test animals. Tail blood (<10 μL) was collected with heparin-coated capillary tubes (Drummond, Broomall, PA) at time points 0, 15, 30, and 90 min from the onset of restraint. Blood samples were centrifuged for 10 min at 5000 rpm to separate plasma for measurement of CORT with an enzyme immunoassay (Enzo Life Sciences, Farmingdale, NY). Statistical analysis was performed by repeated-measures ANOVA and Bonferroni post hoc tests where appropriate. For both males and females in Experiment 1, mice were derived from 6 E-sired and 6 C-sired litters with no more than two mice selected per litter.
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4

Stress-Induced Corticosterone Response

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Eight-week-old male E- and C-sired offspring were subjected to a 15 min restraint stress exposure. All animals were tested between three and five hours after lights on (1000–1200 hr). Briefly, mice were restrained in conical plastic tubes with several air hole perforations near the animal’s head and an opening for the tail. After the 15 minute restraint, each mouse was returned to its home cage. Tail blood (<10ul) was collected with heparin-coated capillary tubes (Drummond, Broomall, PA) at time points 0, 15, 30, and 90 minutes from the onset of restraint. Blood samples were centrifuged for 10 minutes at 4500 × g to separate plasma for measurement of CORT with an enzyme immunoassay (Enzo Life Sciences, Farmingdale, NY). Samples were diluted 1:40 and run in duplicate. The correlation coefficient for duplicate measures in our assay was r= 0.99. The reported sensitivity of this kit for detecting CORT concentrations ranges from 0.032–20 ng/ml. Due to limited animal available, we restricted this experiment to male offspring. Male mice used in this experiment were derived from 8 E-sired litters and 9 C-sired litters.
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