MLPA® - MRC Holland Kits

Please note before download:

  • Mix descriptions are only free of charge for customers with maintenance contract.
  • Don't hesitate to contact us, if there are any mix descriptions missing on this website.
  • To set up a new mix descriptions for you, still available at MRC Hollands website, please provide us the name of the mix (e.g. P002-D1), the version of the mix (e.g. Vs.02) and the date of its release.

  • To set up a new mix descriptions for you, not available at MRC Hollands website any more, please provide us the corresponding document by email or fax (+49-7822-440150-20).

Download

  • log into your SEQUENCE PILOT installation
  • go to category MLPA®
  • go to operation Mixes [master file]
  • press button [Import] and select the downloaded mme-file
  • if the corresponding mix already exists in your SEQUENE_PILOT installation you will be asked "Do you want to save the mix with a new name / lot?"; please press button [Yes] and complete the fields in the following dialogue; press button [OK] to save your entries
  • if the mix doesn't exist yet just press button [OK] in the following dialogue
MIX
VERSION
DATE
REGION
APPLICATION
DOWNLOAD
MIX
P180-B2
VERSION
Vs. 11
DATE
18-03-2014
REGION
Limb malformations, heart
APPLICATION
SALL1 16q12, SALL4 20q13, TBX5 12q24
MIX
P180-B3
VERSION
Vs. 12
DATE
17-02-2016
REGION
Limb malformations, heart
APPLICATION
SALL1 16q12, SALL4 20q13, TBX5 12q24
MIX
P181-A2
VERSION
Vs. 13
DATE
09-12-2012
REGION
Centromeres
APPLICATION
Centromeric screening
MIX
P181-B1
VERSION
Vs. 16
DATE
02-03-2015
REGION
Centromeres
APPLICATION
Centromeric screening
MIX
P182-B1
VERSION
Vs. 13
DATE
09-12-2012
REGION
Centromeres
APPLICATION
Centromeric screening
MIX
P182-B2
VERSION
Vs. 16
DATE
02-03-2015
REGION
Centromeres
APPLICATION
Centromeric screening
MIX
P183-C1
VERSION
Vs. 10
DATE
19-11-2013
REGION
EDA Xq12-q13.1
APPLICATION
Ectodermal dysplasia, x-linked (XLHED)
MIX
P183-C1
VERSION
Vs. 11
DATE
11-07-2017
REGION
EDA Xq12-q13.1
APPLICATION
Ectodermal dysplasia, x-linked (XLHED)
MIX
P184-C2
VERSION
Vs. 11
DATE
10-04-2014
REGION
JAG1 20p12.2
APPLICATION
Alagille Syndrome (AGS)
MIX
P184-C3
VERSION
Vs. 12
DATE
28-04-2017
REGION
JAG1 20p12.2
APPLICATION
Alagille Syndrome (AGS)
MIX
P185-C1
VERSION
Vs. 07
DATE
09-12-2012
REGION
SOX9 17q24.3, NR5A1 9p33, WNT4 1p36.12, NROB1 Xp21.2
APPLICATION
Sex determination
MIX
P185-C2
VERSION
Vs. 09
DATE
19-11-2015
REGION
SOX9 17q24.3, NR5A1 9p33, WNT4 1p36.12, NROB1 Xp21.2
APPLICATION
Sex determination
MIX
P186-C1
VERSION
Vs. 10
DATE
15-07-2015
REGION
PAX3 2q35, MITF 3p14
APPLICATION
Waardenburg syndrome (WS) type II, WS1, WS3
MIX
P186-C2
VERSION
Vs. 11
DATE
14-10-2016
REGION
PAX3 2q35, MITF 3p14
APPLICATION
Waardenburg syndrome (WS) type II, WS1, WS3
MIX
P187-B2
VERSION
Vs. 06
DATE
07-12-2015
REGION
PTCH, SHH, ZIC2, SIX3, TGIF TMEM1, FBXW11
APPLICATION
Holoprosencephaly (HPE)
MIX
P187-B3
VERSION
Vs. 07
DATE
14-11-2017
REGION
PTCH, SHH, ZIC2, SIX3, TGIF TMEM1, FBXW11
APPLICATION
Holoprosencephaly (HPE)
MIX
P188-B2
VERSION
Vs. 10
DATE
21-12-2012
REGION
22q13.3, SHANK3, ACR, RABL2B
APPLICATION
Phelan-Mcdermid syndrome, Telomeric monosomy 22q13.3
MIX
P188-B2
VERSION
Vs. 12
DATE
01-06-2016
REGION
22q13.3, SHANK3, ACR, RABL2B
APPLICATION
Phelan-Mcdermid syndrome, Telomeric monosomy 22q13.3
MIX
P189-C1
VERSION
Vs. 13
DATE
12-10-2015
REGION
CDKL5 Xp22, NTNG1 1p13.3, ARX Xp22.1
APPLICATION
Rett syndrome, atypcial
MIX
P189-C2
VERSION
Vs. 14
DATE
03-03-2017
REGION
CDKL5 Xp22, NTNG1 1p13.3, ARX Xp22.1
APPLICATION
Rett syndrome, atypcial
MIX
P190-C1
VERSION
Vs. 20
DATE
16-08-2016
REGION
CHEK2 22q12, ATM , PTEN, TP53
APPLICATION
Breast cancer suspectibility
MIX
P190-C1
VERSION
Vs. 21
DATE
15-09-2017
REGION
CHEK2 22q12, ATM , PTEN, TP53
APPLICATION
Breast cancer suspectibility
MIX
P190-D1
VERSION
Vs. D1-01
DATE
05-10-2018
REGION
CHEK2 22q12, ATM , PTEN, TP53
APPLICATION
Breast cancer suspectibility
MIX
P191-B2
VERSION
Vs. 12
DATE
15-07-2015
REGION
COL4A5 Xq22
APPLICATION
Alport syndrome, Hereditary Nephritis
MIX
P191-B3
VERSION
Vs. 13
DATE
30-10-2015
REGION
COL4A5 Xq22
APPLICATION
Alport syndrome, Hereditary Nephritis
MIX
P192-B2
VERSION
Vs. 12
DATE
15-07-2015
REGION
COL4A5 Xq22
APPLICATION
Alport syndrome, Hereditary Nephritis
MIX
P192-B3
VERSION
Vs. 13
DATE
30-10-2015
REGION
COL4A5 Xq22
APPLICATION
Alport syndrome, Hereditary Nephritis
MIX
P193-B1
VERSION
Vs. 07
DATE
17-09-2014
REGION
NPC1, NPC2
APPLICATION
Niemann-Pick type C disease (NPC)
MIX
P193-B2
VERSION
Vs. 08
DATE
30-05-2017
REGION
NPC1, NPC2
APPLICATION
Niemann-Pick type C disease (NPC)
MIX
P194-A2
VERSION
Vs. 06
DATE
27-11-2011
REGION
MCCC1 3q27, MCCC2 5q12
APPLICATION
3-methylcrotonylglycinuria I and II
MIX
P194-A2
VERSION
Vs. 07
DATE
10-12-2012
REGION
MCCC1 3q27, MCCC2 5q12
APPLICATION
3-methylcrotonylglycinuria I and II
MIX
P196-B1
VERSION
Vs. 08
DATE
10-12-2012
REGION
TNNT2 1q32
APPLICATION
Hypertrophic cardiomyopathy familial, Dilated cardiomyopathy
MIX
P196-B1
VERSION
Vs. 09
DATE
15-07-2015
REGION
TNNT2 1q32
APPLICATION
Hypertrophic cardiomyopathy familial, Dilated cardiomyopathy
MIX
P197-A2
VERSION
Vs. 11
DATE
15-07-2015
REGION
KCNQ3 8q24.22
APPLICATION
Neonatal convulsions type 2, familial (BFNC2), Epilepsy benign neonatal type 2 (EBN2)
MIX
P197-A3
VERSION
Vs. 12
DATE
25-05-2016
REGION
KCNQ3 8q24.22
APPLICATION
Neonatal convulsions type 2, familial (BFNC2), Epilepsy benign neonatal type 2 (EBN2)
MIX
P198-A2
VERSION
Vs. 08
DATE
10-12-2012
REGION
FH
APPLICATION
Fumarase deficiency (FH)
MIX
P198-A3
VERSION
Vs. 10
DATE
11-03-2015
REGION
FH
APPLICATION
Fumarase deficiency (FH)
MIX
P199-B2
VERSION
Vs. 09
DATE
26-02-2015
REGION
HEXA 15q23
APPLICATION
Tay-sachs disease
MIX
P199-B2
VERSION
Vs. 10
DATE
16-03-2017
REGION
HEXA 15q23
APPLICATION
Tay-sachs disease