Complete Probemix List
Below is the complete overview of all SALSA MLPA probemixes offered by MRC-Holland. You can sort products by article number or application. Please note you can also use the search function above to find a specific gene or application.

Product NameApplicationRegion
A054-Campylobacter MBiT mix 1basic research Genotyping of Campylobacter jejuni isolates Campylobacter
A055-Campylobacter MBiT mix 2basic research Genotyping of Campylobacter jejuni isolates Campylobacter
ME001-Tumour suppressor mix 1basic research Tumour suppressor genes Various
ME002-Tumour suppressor mix 2basic research Tumour suppressor genes Various
ME011-MMRimproved Mismatch repair genes (MMR) MLH1, MSH2, MSH6, PMS2, EPCAM, BRAF V600E
ME024-9p21 Tumours, Cutaneous melanoma 9p21, CDKN2A, CDKN2B
ME028-PWS/AS Prader Willi syndrome (PWS), Angelman syndrome (AS) PWS/AS region (15q11-13), MKRN3, MAGEL2, NDN, SNRPN, UBE3A, ATP10A, GABRB3, OCA2
ME029-FMR1/AFF2 Fragile X FMR1, AFF2
ME030-BWS/RSS Beckwith-Wiedemann Syndrome (BWS), Russell-Silver Syndrome (RSS) 11p15 region, H19, IGF2, CDKN1C, KCNQ1
ME031-GNAS Albright hereditary osteodystrophy (AHO), Pseudohypoparathyroidism (PHP) GNAS 20q13.32
ME032-UPD7-UPD14 Uniparental disomy 6q24, 7p12, 7q32 and 14q32
ME033-TNDM Transient neonatal diabetes mellitus 6q24
ME034-Multi-locus Imprinting Multi-locus imprinting defects and to distinguish maternal and paternal triploidies. 6q24.2; 7q32.2; 11p15.5; 14q32.2; 15q11.2; 19q13.43; 20q13.32 imprinted regions
ME042-CIMPbasic research CpG Island Methylator Phenotype Various
P002-BRCA1CE Hereditary breast cancer (BRCA1) BRCA1 17q21.31
P003-MLH1/MSH2CE Lynch Syndrome MLH1 3p22.2, MSH2 2p21
P008-PMS2CE Lynch Syndrome PMS2 7p22
P010-POLG Mitochondrial maintenance POLG, POLG2, TWNK (C10orf2; PEO1), SLC25A4 (ANT1)
P011-VWF mix 1 Von Willebrand Disease (vWD) vWF 12p13
P012-VWF mix 2 Von Willebrand Disease (vWD) vWF 12p13
P013-ATRX Alpha-Thalassemia/Mental Retardation ATRX ; Xq13
P014-Chromosome 8 Tumour research Chromosome 8
P015-MECP2CE RETT syndrome MECP2, Xq28
P016-VHLCE Von Hippel-Lindau Syndrome VHL, 3p25
P017-MEN1 Multiple endocrine neoplasia MEN1 11q13
P018-SHOXCE Idiopathic growth retardation SHOX-Xp22
P021-SMA Spinal Muscular Atrophy (SMA) SMN1, SMN2, 5q13
P022 -PLP1 Pelizaeus-Merzbacher disease (PMD) PLP1 Xq22
P025-Canavan Canavan disease ASPA, 17p13
P026-Sotos Sotos syndrome NSD1, 5q35
P027-Uveal melanoma Uveal melanoma Chromosome 1p, 3, 6 and 8
P028-FHL Familial lymphohistiocytosis (HLH) UNC13D 17q25.1, PRF1 10q22.1, STX11 6q24.2
P029-WBS Williams-Beuren syndrome WBS criticial region 7q11.23
P031-FANCA mix 1 Fanconi Anemia (FA) FANCA 16q24.3
P032-FANCA mix 2 Fanconi Anemia (FA) FANCA 16q24.3
P033-CMT1CE Charcot-Marie Tooth disease (CMT1), Hereditary Neuropathy with liability to Pressure Palsies (HNPP) CMT1/HNPP region, 17p12
P034-DMD-1CE Duchenne Muscular Dystrophy (DMD) DMD, Xp21.2
P035-DMD-2CE Duchenne Muscular Dystrophy (DMD) DMD, Xp21.2
P036-Subtelomeres Mix 1CE Subtelomeric testing All subtelomeres
P037-CLL-1 Chronic Lymphocytic Leukemia (CLL) Various
P038-CLL-2 Chronic Lymphocytic Leukemia (CLL) Various
P040-CLL Chronic Lymphocytic Leukemia (CLL) Various
P041-ATM-1CE Ataxia-Telangiectasia (AT) ATM 11q23
P042-ATM-2CE Ataxia-Telangiectasia (AT) ATM 11q23
P043-APCCE Hereditary Polyposis Colon Cancer APC, 5q21-q22
P044-NF2 Neurofibromatosis type 2 (NF2) NF2 22q12
P045-BRCA2/CHEK2CE Breast cancer, hereditary BRCA2, CHEK2
P046-TSC2 Tuberous Sclerosis TSC2 16p13.3
P047-RB1 Retinoblastoma (RB) RB1 13q14
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