BETA THALASEMIA MUTATION DETECTION (IVS1-5G-C,619 BP DELETION , cd 8/9 +G, IVS1-1G-T, 41/42-TTCT LAU

BETA THALASEMIA MUTATION DETECTION (IVS1-5G-C,619 BP DELETION , cd 8/9 +G, IVS1-1G-T, 41/42-TTCT LAUNCHING IN INDIA

WE ARE PRIVILLEGED TO ANNOUCED THE LAUNCHING OF THE ABOVE SAID TEST IN INDIA.,

THE PROCEDURE MULTIPLEX PCR.
CONTIANER TYPE AMINOTIC FLUID/CVS IN STERILE TISSUES CULTURE MEDIA
OR
SALINE / FETAL BLOOD IN EDTA+EDTA WHOLE BLOOD FOR BOTH

REPORT TIME:8DAYS FROM THE DATE OF RECEIPT OF THE SAMPLE TO OUR LAB.
PRICES :SHALL INFORM WHEN YOU CONTACT US .

INTRODUCTION :
The most common inherited diseases in humans result from mutations in the beta-globin gene com-plex and the alpha-globin gene complex. We refer
to the beta-globin gene complex as
HBBC
, com- posed of the genes HBE1 (MIM# 142100), HBG2(MIM# 142250), HBG1(MIM# 42200), HBD(MIM# 142000), and HBB (MIM# 141900),which encode the epsilon-, Ggamma-, Agamma-,delta-, and beta-globin polypeptides, respectively.We refer to he alpha-globin gene complex asHBAC, composed of the genes HBZ2 (MIM#142310), HBA2(MIM# 141850), HBA1(MIM#141800), and HBQ1 (MIM# 142240), which en-code the zeta-, alpha2-, alpha1-, and possibly theta-
globin polypeptides, respectively.