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If we desire to determine the greatly ordinary beta-thalassemia modifications and the hemoglobin variants then we should utilize TBGGS. Dominant beta-thalassemia and hyper hazardous Hb variants as well as further Hb variants are specified by it.
TBGGS cannot detect numerous Hb ailments such as crossover circumstances and large deletional modifications. The arrangement of its outcome is accomplished within the context of RBC indices and polypeptide analyses.
TBGGS orders numerous assortments of methods. These practices are examined in the following technique
TBGGS demands a DNA specimen. We should not brush the specimen emanating from the body of the patient.
The utility can be consulted in the following method.
In the scheme, TBGGS, foremost of all, a DNA instance is prepared. For equipping a DNA specimen, the specimen is put up with from the cheek, hair, or saliva. That specimen is authorized to be split up into two facets. We have to remove DNA from that specimen and have to clarify it. We can catch sight of common beta-thalassemia modifications in the DNA specimen of Patients by sequencing technology.
Hemoglobin electrophoresis is utilized to analyze beta-thalassemia. Hereditary experimenting is utilized to analyze alpha thalassemia.
Two percent-Three percent
Ordinary Consequences
HbA2: 2% to 3%
Test Type | Beta Thalassemia: HBB Gene Sequencing |
Includes | Beta Thalassemia: HBB Gene Sequencing (Pathology Test) |
Preparation | |
Reporting | Within 24 hours* |
Test Price |
₹ 7500
|
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