The Microbe is a multi-speciality diagnostic laboratory established by a group of women entrepreneurs under the leadership of Dr Sharayu Gaikwad and Ms Vinita Dhoot. It provides a wide spectrum of diagnostic tests encompassing biochemistry, microbiology, cytopathology, histopathology, immunology, etc., with reliable and highly accurate reports. We believe in open communication and are available with a willing ear for report discussion.

The Microbe Lab

Gene-Deletion/duplication ABCB4

Gene-Deletion/duplication ABCD1Â

Gene-Deletion/duplication Androgen receptor (AR)

Gene-Deletion/duplication Ataxia-telangiectasia (ATM)

Gene-Deletion/duplication Canavan disease (ASPA)

Gene-Deletion/duplicationCharcot-Marie-Tooth and 1A/HNPP (PMP22, COXI0, TEKT3)

Gene-Deletion/duplication Charcot-Marie-Tooth PMP22

Gene-Deletion/duplicationCharcot-Marie-Tooth type 4 (EGR2, GDAP1, NEFL, PRX)

Gene-Deletion/duplication choroideremia - CHM gene

Gene-Deletion/duplication Congenital adrenal hyperplasia CYP21A2 (21-0H)

Gene-Deletion/duplication Congenital Muscular Dystrophy (LAMA2)

Gene-Deletion/duplication Cystic megalencephaly (MLC1)

Gene-Deletion/duplication DCX gene for isolated lissencephaly sequence

Gene-Deletion/duplication Dravet syndrome (SCN1A)

Gene-Deletion/duplication Dysferlinopathy/LGMD2A (CAPN3)

Gene-Deletion/duplication Dysferlinopathy/LGMD2B (DYSF)

Gene-Deletion/duplication Early infantile epileptic encephalopathy-4

Gene-Deletion/duplication Fabry disease (GLA)

Gene-Deletion/duplication GLUT1 deficiency (SLC2A1)

Gene-Deletion/duplication Glycine encephalopathy (GLDC)

Gene-Deletion/duplication Haemophilia (F8)

Gene-Deletion/duplication Hemolytic uremic syndrome

Gene-Deletion/duplication Hemophagocytic

Gene-Deletion/duplication Hyper-immunoglobulin Esyndrome(DOCK8, STAT3)

Gene-Deletion/duplication Krabbe disease (GALC)

Gene-Deletion/duplicationLimb-girdle muscular dystrophy (SGCA, SGCB,SGCD, SGCG & FKRP)

Gene-Deletion/duplication Lynch syndrome (MLH1, MSH2, EPCAM)

Gene-Deletion/duplication Menkes disease (ATP7A)

Gene-Deletion/duplication Multiple exostoses (EXT1 & EXT2)

Gene-Deletion/duplication Neurofibromatosis type 2 (NF2)

Gene-Deletion/duplication Neurometabolic disorder (MLC1,L2HGDH,D2HGDH, MLYCD)

Gene-Deletion/duplication Neuronal ceroid lipofuscinosis  deficiency

Gene-Deletion/duplication NF1

Gene-Deletion/duplication Niemann Pick disease (NPC1, NPC2, SMPD1)

Gene-Deletion/duplication OTC

Gene-Deletion/duplication Pantothenate kinase-associated

Gene-Deletion/duplication Pantothenate kinase-associatedneurodegeneration (PLA2G6)

Gene-Deletion/duplication Polycystic kidney disease (PKHD1) deficiency

Gene-Deletion/duplication Pompe disease (GAA)

Gene-Deletion/duplication Propionic acidemia (PCCA) deficiency

Gene-Deletion/duplication Protein S deficiency (PROS1 gene   )

Gene-Deletion/duplication RB1 gene

Gene-Deletion/duplication Rett Syndrome (MECP2)

Gene-Deletion/duplication Sotos syndrome (NSD1)

Gene-Deletion/duplication Tay-Sachs disease (HEXA)

Gene-Deletion/duplication TP53 gene Large   - MLPA

Gene-Deletion/duplication TSC1

Gene-Deletion/duplication TSC2

Gene-Deletion/duplication Usher syndrome (USH2A)

Gene-Deletion/duplication WAGR syndrome (PAX6)

Gene-Deletion/duplication Wilson disease (ATP7B)

Gene-Deletion/duplication X-linked spastic paraplegia-2 (PLP1)

The ALL Panel Deletion/Duplication Detection blood test detects genetic abnormalities such as deletions or duplications in the DNA associated with acute lymphoblastic leukemia (ALL). This test aids in diagnosing ALL and determining appropriate treatment strategies based on the genetic profile of the cancer cells.

ALL Panel Deletion/Duplication Detection

ALL Panel Deletion/Duplication Detection

About This Test

The Microbe Lab

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