Rat Insulin RIA


This Rat Insulin Radioimmunoassay (RIA) Kit is for the quantitative determination of Rat Insulin in serum, plasma, and other tissue culture media. The primary antibody was raised in guinea pigs against highly purified Rat Insulin. Sensitivity of 0.1 ng/ml can easily be achieved when using a 100 m l serum or plasma sample in an overnight, equilibrium assay (300 m l Total Volume). An alternative room temperature incubation for two hours may be used to shorten the assay to provide results within one day. This kit is for research purposes only.


In radioimmunoassay, a fixed concentration of labeled tracer antigen is incubated with a constant dilution of antiserum such that the concentration of antigen binding sites on the antibody is limited, for example, only 50% of the total tracer concentration may be bound by antibody. If unlabeled antigen is added to this system, there is competition between labeled tracer and unlabeled antigen for the limited and constant number of binding sites on the antibody. Thus, the amount of tracer bound to antibody will decrease as the concentration of unlabeled antigen increases. This can be measured after separating antibody-bound from free tracer and counting one or the other, or both fractions.

A standard curve is set up with increasing concentrations of standard unlabeled antigen and from this curve the amount of antigen in unknown samples can be calculated. Thus, the four basic necessities for a radioimmunoassay system are: a specific antiserum to the antigen to be measured, the availability of a radioactive labeled form of the antigen, a method whereby antibody-bound tracer can be separated from the unbound tracer, and finally, an instrument to count radioactivity. The Linco Research Rat Insulin assay utilizes 125I-labeled insulin and a Rat Insulin antiserum to determine the level of Rat Insulin in serum, plasma or tissue culture media by the double antibody/PEG technique.


Each kit is sufficient to run 250 tubes and contains the following reagents.

A. Assay Buffer

0.05M Phosphosaline, pH 7.4, containing 0.025M

EDTA, 0.08% Sodium Azide, and 1% RIA Grade BSA

Quantity: 40 ml/vial

Preparation: Ready to use

B. Rat Insulin Antibody

Guinea Pig anti-Rat Insulin Serum in Assay Buffer

Quantity: 26 ml/vial

Preparation: Ready to use

C. 125I-Insulin

125I-Insulin Label, HPLC purified (specific

activity 367 µCi/µg)

Lyophilized for stability. Freshly iodinated label

contains <5 µCi (<185 kBq), calibrated to the 1st Monday of each month.

Quantity: 27 ml/vial upon hydration

Preparation: Contents Lyophilized. Hydrate with entire contents of Label Hydrating Buffer. Allow to sit at room temperature for 30 minutes, with occasional gentle mixing.

D. Label Hydrating Buffer

Assay Buffer containing Normal Guinea Pig IgG as carrier. Use the entire content to hydrate


Quantity: 27 ml/vial

Preparation: Ready to use

E. Rat Insulin Standards

Purified Rat Insulin in Insulin Standard Buffer at the following concentrations:

0.1, 0.2, 0.5, 1.0, 2.0, 5.0, 10.0 ng/ml

Quantity: 1 ml/vial

Preparation: Ready to use

F. Quality Controls 1 & 2

Purified Rat Insulin in Assay Buffer

Quantity: 1 ml/vial

Preparation: Ready to use

G. Precipitating Reagent

Goat anti-Guinea Pig IgG Serum, 3% PEG and 0.05% Triton X-100 in 0.05M Phosphosaline, 0.025M EDTA, 0.08% Sodium Azide

Quantity: 260 ml/vial

Preparation: Ready to use, chill to 4°C


Refrigerate all reagents between 2 and 8°C for short term storage. For prolonged storage (>2 weeks), freeze at £ -20°C. Avoid multiple (>5) freeze/thaw cycles. Refer to date on bottle for expiration when stored at £ -20°C. Do not mix reagents from different kits unless they have the same lot number.


A. Radioactive Materials

This radioactive material may be received, acquired, possessed and used only by research personnel or clinical laboratories for in vitro research tests not involving internal or external administration of the material, or the radiation therefrom, to human beings or animals. Its receipt, acquisition, possession, use and transfer are subject to the regulations of the U. S. Nuclear Regulatory Commission (NRC) or of a State with which the Commission has entered into an agreement for the exercise of regulatory authority.

The following are suggested general rules for the safe use of radioactive material. The customer’s Radiation Safety Officer (RSO) is ultimately responsible for the safe handling and use of radioactive material.

1. Wear appropriate personal devices at all times while in areas where radioactive materials are used or stored.

2. Wear laboratory coats, disposable gloves, and other protective clothing at all times.

3. Monitor hands, shoes, clothing and immediate area surrounding the workstation for contamination after each procedure and before leaving the area.

4. Do not eat, drink, or smoke in any area where radioactive materials are stored or used.

5. Never pipette radioactive material by mouth.

6. Dispose of radioactive waste in accordance with NRC rules and regulations.

7. Avoid contaminating objects such as telephones, light switches, doorknobs, etc.

Use absorbent pads for containing and easily disposing of small amounts of contamination.

9. Wipe up all spills immediately and thoroughly and dispose of the contaminated materials as radioactive waste. Inform Radiation Safety Officer.

B. Sodium Azide

Sodium Azide has been added to all reagents as a preservative at a concentration of 0.08%. Although it is at a minimum concentration, Sodium Azide may react with lead and copper plumbing to form highly explosive metal azides. On disposal, flush with large volume of water to prevent azide build up.


1. Borosilicate glass tubes, 12 x 75 mm. (NOTE: Polypropylene or polystyrene tubes may be used if the investigator finds that the pellet formation is acceptably stable in their system.)

2. 100 µl pipette with disposable tips

3. 100 µl & 1.0 ml repeating dispenser

4. Refrigerated swing-bucket centrifuge capable of developing 2,000 - 3,000 xg. (Use of fixed-angle buckets is not recommended.)

5. Absorbent paper

6. Vortex mixer

7. Refrigerator

8. Gamma Counter


1. A maximum of 100 µl per assay tube of serum or plasma can be used, although 50 µl per assay tube is adequate for most applications. Tissue culture and other media may also be used.

2. Care must be taken when using heparin as an anticoagulant, since an excess will provide falsely high values. Use no more than 10 IU heparin per ml of blood collected.

3. Specimens can be stored at 4°C if they will be tested within 24 hours of collection. For longer storage, specimens should be stored at £ -20°C. Avoid multiple (>5) freeze/thaw cycles.

4. Avoid using samples with gross hemolysis or lipemia.


For optimal results, accurate pipetting and adherence to the protocol are recommended.

A. Assay Set-Up, Day One

1. Pipette 200 µl of Assay Buffer to the Non-Specific Binding (NSB) tubes (3-4) and 100 µl to Reference (Bo) tubes (5-6). No buffer is added to tubes 7 through the end of the assay.

2. Pipette 100 µl of Standards and Quality Controls in duplicate (see flow chart).

3. Pipette 100 µl of each sample in duplicate.

(NOTE: Smaller volumes of sample may be used when Insulin concentrations are anticipated to be elevated or when sample size is limited. Additional Assay Buffer should be added to compensate for the difference so that the volume is equivalent to 100 µl, e.g., when using 50 µl of sample, add 50 µl of Assay Buffer). Refer to Section IX for calculation modification.

4. Pipette 100 µl of hydrated 125I-Insulin to all tubes. Important: For preparation, see Section III, Part C.

5. Pipette 100 µl of Rat Insulin antibody to all tubes except Total Count tubes (1-2) and NSB tubes (3-4).

6. Vortex, cover, and incubate overnight (20-24 hours) at 4° C.

NOTE: As an alternative, this assay may be shortened at this step to an incubation time of 2 hours when incubated at room temperature 20-25°C.

B. Day Two

7. Add 1.0 ml of cold (4°C) Precipitating Reagent to all tubes except Total Count tubes (1-2).

8. Vortex and incubate 20 minutes at 4°C.

9. Centrifuge, 4°C, all tubes except Total Count tubes (1-2) for 20 minutes at 2,000-3,000 xg. NOTE: If less than 2,000 xg is used or if slipped pellets have been observed in previous runs, the time of centrifugation must be increased to obtain a firm pellet (e.g., 40 minutes). Multiple centrifuge runs within an assay must be consistent.

Conversion of rpm to xg:

xg = (1.12 x 10-5) (r) (rpm)2

r = radial distance in cm (from axis of rotation to the bottom of the tube)

rpm = revolutions per minute

10. Immediately decant the supernatant of all tubes except Total Count tubes (1-2), drain tubes for at least 15-60 seconds (be consistent between racks), and blot excess liquid from lip of tubes. NOTE: Invert tubes only one time. Pellets are fragile and slipping may occur.

11. Count all tubes in a gamma counter for 1 minute. Calculate the ng/ml of Rat Insulin in unknown samples using automated data reduction procedures (see Section IX).