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Laboratory of Synapse Structure and Function | |||||
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Materials: lead nitrate, sodium citrate, 1 N sodium hydroxide
solution (aqueous), 50 ml graduated cylinder, 1000 ml Erlenmeyer flask, 2X
distilled water, plastic transfer pipettes, 50 ml volumetric flask, top loading
balance, 10 ml graduated plastic pipette, nitric acid, 5 ten ml capacity
syringes, 26 gauge hypodermic needles, small rubber cork, paper tape, lab coat
and/or apron, surgical mask, gloves, goggles.
Procedure:
1.
Fill
all glassware with 10% nitric acid (aqueous) for several minutes. Then discard
the solution into appropriate waste container. Rinse the glassware at least 10X
with twice distilled water. Set aside to dry. This nitric acid solution really
clean/etches all glassware!
2.
Boil
about 750 ml of double distilled water in 1000 ml Erlenmeyer on hotplate for at
least 30 minutes in order to boil off carbon dioxide. Continue to boil through
out procedure.
3.
Next,
weigh out 1.33 grams of lead nitrate and carefully add to 50 ml volumetric
flask.
4.
Add
30 ml of the boiled water to the 50 ml volumetric flask and shake.
5.
Add
1.76 grams of sodium citrate to 50 ml volumetric flask.
6.
Shake
vigorously for 2 minutes. Solution will be a milky white.
7.
Let
stand 30 minutes with occasional shaking by inversion.
8.
Add
8 ml of 1 N sodium hydroxide solution (freshly made). Mix by inversion. The
solution should clear.
9.
Bring
up the volume to 50 ml.
10.
Dispense
the lead citrate into 10 ml portions into each of the syringes. Cap with a
hypodermic needle.
11.
Expel
any air in syringe.
12.
Place
the syringes, hypodermic needle down into the rubber cork and place all in a
plastic 200 cc cup for storage. Store in refrigerator (4 degree C). Label the
cup with today's date with tape or magic marker.
| Last Updated: 5/17/01 |