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Experiments list


Medical diagnosis Hormone Row Name tests
1 T3
2 T4
3 T3 up
4 TSH
5 Beta HCG Titer
6 FSH
7 LH
8 Prolactin
9 Inhibin A
10 Free estriol
11 Free BHCG
12 Papp A
13 AFP
Immunology 14 HBs Ag
15 HCVAb
16 HIV1,2
17 HTLV1,2
18 Toxoplasmosis (IgG-IgM)
19 Rubella (IgG-IgM)
20 Anti phospholipid (IgG-IgM)
21 Anti Cardiolipin (IgG-IgM)
22 Anti TPO
23 ANA
Serology 24 ASO
25 CRP
26 CRP Titer
27 RF
28 Wright
29 Widal
30 2ME
31 Coombs Wright
32 RPR
33 PPD
Medical diagnostic Hematology Row Name tests
34 CBC
35 BT
36 CT
37 PT
38 PTT
39 BG & Rh
40 Coombs Direct & Indirect
41 LE Cell
42 Malaria
43 Retic
44 G6PD
45 Hb Electrophoresis
46 Protein Electrophoresis
Biochemistry 47 FBS
48 BS2hpp
49 GCT
50 GTT
51 Bun
52 Cr
53 Urea
54 Uric Acid
55 HDL
56 LDL
57 CPK
58 Triglyceride
59 Cholestrol
60 SGOT
61 SGPT
62 TIBC
63 Calcium
64 Phosphorous
65 Fe
66 LDH
67 ALP
Medical diagnostic Biochemical urine Row Name tests
68 Urine Volume/24hr
69 Urea 24hr
70 Protein 24hr
71 Ca 24hr
72 Phoaphorous 24hr
73 Uric Acid 24hr
74 Creatinine 24hr
Microbiology 75 U/A
76 U/C
77 Stool Culture
78 Throat Culture
79 Ear Culture
80 Sputum Culture
81 Vaginal Culture
82 Urethral Culture
83 Nasal Culture
84 Prostate Culture
85 Leishman
86 Fungi
87 Scabies
88 Erythrasma
89 Demodex
90 Pityrosporum1
Screening tests in pregnancy 91 Double Marker
92 Triple Marker
93 Quad Marker
medical Genetics Cytogenetic Row Name tests
1 Get blood karyotype
2 Preparation karyotype of amniotic fluid
3 Karyotype prepared from aborted fetal tissue
4 FISH
Molecular Genetics 5 Hydroxy glutaric
6 Inclusion Cell (Icell disease)
7 LAFORA
8 PND (Alpha and beta thalassemia and hemophilia, etc.)
9 Duchenne
10 Iterations diseases such as Fragile X Syndrome Huntington dystrophy, /Spinocerebllar Ataxia friedreich ataxia
11 SMA (I, II)
12 Gitelman syndrome
13 syndrome Rett
14 Milroy disease
15 syndrome TAR
16 Prenatal diagnosis of Duchenne x fragile
17 FMF
18 TAR Syndrome
19 Microcephaly
20 GjB2/GJB3/GJB6
21 MMA Asydmya
22
23 Thrombophilia (RPL) FV/F II/ MTHFR/PAII
24 G6PD
25 Angelman syndrome
26 MCAD
27 PKU
28 Batten disease
29 Achondroplasia
30 Hereditary Spastic Paraplegia
31 Joubert syndrome
medical Genetics Molecular Genetics 32 DMD-MLPA
33 CGH Array
34 Determine paternity test
35 cystic fibrosis
36 Panel Hearing
37 Coagulation deficiency (hemophilia A and B)
38 QF PCR
39 Mucopolysaccharidosis type (Type II, Type III, Type IV, Type VI, etc.)
40 Achondroplasia
41 Charcot-Marie-Tooth disease
42 Tay-Sachs disease
43 Propionic acid
44 Loco metachromatic dystrophy ( ARSA Deficiency)
45 Ataxia telangiectasia
46 Alpha and beta thalassemia
47 Paternity test