1. Practical Clinical Hematology5
Hemoglobin A2

2. Introduction
HBA2 is a protein which in humans is encoded by the HBA2 gene.
Hemoglobin A2 is a normal variant of hemoglobin A that consists of two alpha and two delta chains and is found in small quantity in normal human blood.
Normal value of HBA2 in the adult is
( 1.8 – 3.5%).
Cytogenetic Location: 16p13.3
More precisely, the HBA2 gene is located from base pair 222,845 to base pair 223,708 on chromosome 16

3. HbA2 elevated up to 8% indicates: β. Thalassemia trait
Homozygous Thalassemia
Decreased level may be found in:
Iron deficiency anemia.
Hb H disease.
Hereditary persistence of Hb F.
Fibroblastic anemia.
Carriers of α Thalassemia.
Elevated levels ( %) of Hb A2 are seen with beta thalassemia trait. Several abnormal hemoglobins including Hb S, E, C and O may cause spurious elevation. Hb A2 may be increased with megaloblastic anemia and decreased with iron deficiency anemia. 

4. HbA2 test
The anion exchange micro chromatography procedure is an accurate and easily performed method for HbA2 Quantization.
Principle:
A hemolysate is prepared from the patients red blood cells.
A specific amount of hemolysate is then added to the top of the resin column.
The diethyl amino ethyl (DEDE) resin is a preparation of cellulose attached to positively charged molecules, The positively charged cellulose attracts negatively charged molecules
The anion exchange resin is a preparation of cellulose covalently coupled to small positively charged molecules.
Proteins, such as the hemoglobins, contain many positive and negative charges due to the ionizing properties of the component amino acids
buffer and pH levels are controlled to cause different hemoglobins to possess different net negative charges.

5. Principle
When the hemolysate is added to the column, the PH of the buffer present determines the net negative charge of the Hb, which then binds to the positively charged cellulose resin.
The Hb are selectively removed from cellulose according to the PH of the developer.
The proteins are removed selectively from the resin by altering the pH or ionic strength of the elution buffer.
Due to the pH of the resin and the ionic strength of the HbA2 Developer, HbA2 does not bind to the positively charged cellulose and is eluted as the developer moves through the column.

6. In this procedure the HbA2 (originally bound to the resin) is released from the resin and eluted by the developer as it passes through the column.
Most other normal and abnormal HbS remain bound to the resin in the column.
The eluted HbA2 is then measured spectrophotometrically and compared with the amount of total Hb in the specimen to calculate the percent of HbA2 present.

7. Procedure Hemolysate preparation: Blood 50 µl. Distilled water 200 µl.
Good mixing and leaved it for some time at R.T.

8. Separation and reading HbA2
Remove the upper of the Micro column and then snap the tip off the bottom. Then, using the rounded end of a pipette, push the upper disc down to resin surface taking care not to compress it. Let the micro column drain completely to waste.
Take 50 µl from hemolysate and put it on the upper disc and let the column drain to waste.
Add 200 µl from reagent (1) buffer and put it on the upper disc and let the column drain to waste.
Place the micro column over a test tube and add 3.0 ml from developer.
Collect the elute ( Hb A2 fraction)

9. Shake thoroughly and read absorbance (Abs) of the HbA2 fraction at 415 nm against distilled water (Abs HbA2)

10. Reading of total hemoglobin
Put in test tube 12.0 ml distilled water and 50 µl hemolysate and then read at 415nm against distilled water.

11. Calculation

12. Today Lab:

13. The reagents are stable up to the expiry date stated on the labels, if stored at 15-25 °C.
Strong temperature variations may alter resin equilibrium and consequently its functionality; if erroneously stored at 2-8 °C the resin has to remain at room temperature for at least three days before using.
Tubes containing yellowish-white resin indicate chemical degradation and cannot be used.

14. The hemolisate is directly placed in the test tubes containing DEAE-cellulose resin. Hemoglobin A2 unlike all remaining hemoglobin is not linked by the resin and then can be separated by means of special separating filters.

15. Dispense into tube 300 μl Lysing Solution (Reagent B).
Place 50 μl of the well-mixed blood sample.
Mix well and allow to stand for 5 minutes.

16. Add 100 μl of the hemolysate in the resin tube (RA).
Position the Filter Separators in the tubes so that the rubber sleeve is approximately 1 cm above the liquid level.
Place the tubes on the rocker or rotator and gently mix continuously for 5 minutes (alternatively turn upside down at least six times at intervals of one minute).
Remove the tubes from the rocker or rotator. Push the Filter Separator into the tubes proceeding slowly until the resin is firmly packed.

17. The supernatant may be poured into another tube or directly into a cuvette for absorbance measurement.
Read the absorbance values at 415 nm against a reagent blank made of liquid phase obtained from a test tube without hemolysate (A HbA2).

18. Pipette in empty test tube (Hb Total) 100 µl from hemolisate and 5 ml from distilled water.
Mix and read the absorbance against a reagent blank made of distilled water at 415 nm.

19. Calculation