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Sickle Cell Anemia (HbS) MutationAnalysis (β6 Glu-Val )

 

DESCRIPTION – sickle hemoglobin is a result of a point mutation in the beta globin chain. This point mutation replaces A with T at codon of beta hemoglobin chain. This causes the switch from glutamic acid to valine amino acid. The valine type hemoglobin causes red cells to sickle when exposed to a low oxygen threshold

METHODOLOGY – polymerase chain reaction (PCR)

TURN AROUND TIME – 8 days

PATIENT PREPARATION –

COLLECT – lavender (EDTA), pink (potassium EDTA), yellow (ACD solution A or B)

SPECIMEN PREPARATION – transport 3 ml whole blood

STORAGE/TRTANSPORT TEMPERATURE – refrigerated

STABILITY – ambient: 72 hours; refrigerated: 1 week

MRP 2700.00

SPECIAL INSTRUCTIONS – clinical history is mandatory

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Get Report In
8th day
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Pre-Test Information
3 ml of EDTA Whole Blood
2,700.00
Home Collection-
Offer Price2,700.00
Total Amount₹2,700.00
*inclusive of all the taxes, fees and subject to availability

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