microCLEAN PCR purification provides a simple spin protocol that is quicker, cheaper and more flexible than other products. It offers excellent recovery, is reliable and can be used for both tubes and plates. Just add an equal volume of microCLEAN to the sample, follow the 1½ spin protocol and get clean PCR fragments/DNA in less than 15 minutes.

microCLEAN1 ml2MCL-1datadata
microCLEAN5 x 1 ml2MCL-5datadata
microCLEAN10 x 1 ml2MCL-10datadata
microCLEAN1 x 50 ml2MCL50datadata

For a full list of microCLEAN citations please see the link below:

  • microCLEAN citations
      2015A Homozygous Nonsense Thyroid Peroxidase Mutation r540x Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family
      2015In vitro comparison of the effect of two factor XI (FXI) concentrates on thrombin generation in major FXI deficiency
      2015Generation and Characterization of a Transgenic Mouse Carrying a Functional Human-Globin Gene with the IVSI-6 Thalassemia Mutation
      2015Phylogenetic approach of the section Bulbocodii DC of Narcissus based on cpDNA. A case of taxonomic inflation?
      2015Fructan synthesis, accumulation and polmer traits. II. Fructan pools in populations of perennial ryegrass (Lolium perenne L.) with variation for water-soluble carbohydrate and candidate genes were not correlated with biosynthetic activity and demonstrated constraints to polymer chain extension
      2015A novel multiplex assay for simultaneously analysing 13 rapidly mutating Y-STRs
      2015Not so sluggish: the success of the Felimare picta complex (Gastropoda, Nudibranchia) crossing Atlantic biogeographic borders
      2015Dispersal constraints and fine-scale spatial genetic structure in two earthworm species
      2015A new Parougia species (Annelida, Dorvilleidae) associated with eutrophic marine habitats in Antarctica
      2015Hepatitis B virus genotype and subgenotype prevalence and distribution in Montenegro
      2015The Missense Alteration A5T of the Thyroid Peroxidase Gene is Pathogenic and Associated with Mild Congenital Hypothyroidism
      2015Protein O-mannosylation is crucial for human mesencyhmal stem cells fate
      2015A rare mutation in MYH7 gene occurs with overlapping phenotype
      2014Genetic Structure of Earthworm Populations at a Regional Scale: Inferences from Mitochondrial and Microsatellite Molecular Markers in Aporrectodea icterica (Savigny 1826)
      2014An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis
      2014A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism
      2014Analysis of a potential cluster of rhinovirus infections in patients and staff on two haemato-oncology wards
      2014Respiratory outcome of prematurely born infants following human rhinovirus A and C infections
      2014Late-adult onset of X-linked myopathy with excessive autophagy (XMEA)
      2013Novel truncating thyroglobulin gene mutations associated with congenital hypothyroidism
      2013Patient characteristics and severity of human rhinovirus infections in children
      2013Development of novel real-time TaqMan® PCR assays for the species and sex identification of otter (Lutra lutra) and their application to noninvasive genetic monitoring
      2013Combined Molecular and Morphological Phylogenetic Analyses of the Blakeeae (Melastomataceae)
      2013The effect of clozapine on mRNA expression for genes encoding G protein-coupled receptors and the protein components of clathrin-mediated endocytosis
      2012Genetic Mapping of Genes Involved in Autosomal Recessive Mental Retardation
      2012Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community
      2012PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutations
      2012Genetic signature of accidental transfer of the peregrine earthworm Pontoscolex corethrurus (Clitellata, Glossoscolecidae) in French Guiana
      2012Early-onset Lafora body disease
      2012Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease
      2012Lineages, Sub-Lineages and Variants of Enterovirus 68 in Recent Outbreaks
      2012Isolation of polymorphic microsatellite markers in Aporrectodea icterica (Savigny 1826)
      2012Global Analysis of Gene Expression in the Developing Brain of Gtf2ird1-/- Mice
      2012Analysis of LIN28A in early human ovary development and as a candidate gene for primary ovarian insufficiency
      2011Pasteuria endospores from Heterodera cajani (Nematoda: Heteroderidae) exhibit inverted attachment and altered germination in cross-infection studies with Globodera pallida (Nematoda: Heteroderidae)
      2011Use of Robotics in High-Throughput DNA Sequencing
      2011Identification of New Single Nucleotide Polymorphism-Based Markers for Inter- and Intraspecies Discrimination of Obligate Bacterial Parasites (Pasteuria spp.) of Invertebrates
      2011The Lusitania Province as a center of diversification: The phylogeny of the genus Microlipophrys (Pisces: Blenniidae)
      2011Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome
      2011Clonal structure of Streptococcus sanguinis strains isolated from endocarditis cases and the oral cavity
      2011Facultative methylotrophs from the human oral cavity and methylotrophy in strains of Gordonia, Leifsonia, and Microbacterium
      2010Henrietteeae (Melastomataceae): A New Neotropical Berry-Fruited Tribe
      2010A method for release and multiple strand amplification of small quantities of DNA from endospores of the fastidious bacterium Pasteuria penetrans
      2010Occurrence of Pythium aphanidermatum Root and Collar Rot of Papaya (Carica papaya L.) in Côte d'Ivoire
      2010Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism
      2010A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse
      2010PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit
      2010High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta
      2010Generation of Diversity in Streptococcus mutans Genes Demonstrated by MLST
      2009HECTD2 Is Associated with Susceptibility to Mouse and Human Prion Disease
      2009The heritability and genetics of frontotemporal lobar degeneration
      2009Shadoo (Sprn) and prion disease incubation time in mice
      2009Steinernema australe n. sp. (Panagrolaimomorpha: Steinernematidae), a new entomopathogenic nematode from Isla Magdalena, Chile
      2009Production of Poly-α-hydroxybutyrate (PHB) from Sago Starch by The Native Isolate Bacillus megaterium PSA10
      2009Population structure of Streptococcus oralis
      2009Divergence, hybridization, and recombination in the mitochondrial genome of the human pathogenic yeast Cryptococcus gattii
      2009Patrilocality and recent migrations have little impact on shaping patterns of genetic structure of the armenian population
      2008Investigation of Mcp1 as a Quantitative Trait Gene for Prion Disease Incubation Time in Mouse
      2008Long-distance dispersal and recombination in environmental populations of Cryptococcus neoformans var. grubii from India
      2008Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues
      2008Polyphyly across oceans: a molecular phylogeny of the Chromodorididae (Mollusca, Nudibranchia)
      2008Mutation analysis of haemophilia B in the Irish population: increased prevalence caused by founder effect
      2008A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
      2008A motif in the C-terminal domain of ϕC31 integrase controls the directionality of recombination
      2007Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution
      2007Aggregating Phenotype in Lactobacillus crispatus Determines Intestinal Colonization and TLR2 and TLR4 Modulation in Murine Colonic Mucosa
      2007Peptidyl argininedeiminase 2 CpG island in multiple sclerosis white matter is hypomethylated
      2006Duplication and relocation of the functional DPY19L2 gene within low copy repeats
      2006Identification of genes expressed in the accessory glands of male Mediterranean Fruit Flies (Ceratitis capitata)
      2006A naturally occurring epigenetic mutation in a gene encoding an SBP-box transcription factor inhibits tomato fruit ripening
      2006ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
      2006Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands
      2005Novel DNA Sequences from Natural Strains of the Nitrogen-Fixing Symbiotic Bacterium Sinorhizobium meliloti
      2005OrageneTM DNA and DNA sequencing with ABI PRISM®
      2005Post-mortem DNA damage hotspots in Bison (Bison bison) provide evidence for both damage and mutational hotspots in human mitochondrial DNA
      2005Mutational screening and association study of glutamate decarboxylase 1 as a candidate susceptibility gene for bipolar affective disorder and schizophrenia
      2004Identification and characterization of a novel mouse prion gene allele
      2004Progressive myoclonus epilepsy with polyglucosans (Lafora disease)
      2004Mutation Scanning for the Clinical Laboratory DHPLC
      2003Distribution Patterns of Postmortem Damage in Human Mitochondrial DNA
      2003The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome
      2003No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders
      2002Typing of multiple single nucleotide polymorphisms in cytokine and receptor genes using sNaPshot
      2002Founding Mothers of Jewish Communities: Geographically Separated Jewish Groups Were Independently Founded by Very Few Female Ancestors

For a full list of microCLEAN reviews please see the link below:

  • microCLEAN reviews
      2006MicroClean From Microzone Ltd.
      2006OrageneTM And DNA Sequencing With ABI Prism®

If you are interested in finding out what other papers our products have been cited in, please see our dedicated citations page.