Related Experiment Video

Updated: Aug 15, 2026

Chemically-blocked Antibody Microarray for Multiplexed High-throughput Profiling of Specific Protein Glycosylation in Complex Samples
13:21

Chemically-blocked Antibody Microarray for Multiplexed High-throughput Profiling of Specific Protein Glycosylation in Complex Samples

Published on: May 4, 2012

No evidence for an association between glyoxalase I and haptoglobin in nine Spanish populations

M M de Pancorbo, A Garcia-Orad

    Human Heredity
    |January 1, 1987
    PubMed

    Abstract:

    No association between glyoxalase I and haptoglobin phenotypes was found in 9 Spanish populations. This is in accordance with two out of three papers published.

    More Related Videos

    Detecting Glycogen in Peripheral Blood Mononuclear Cells with Periodic Acid Schiff Staining
    09:42

    Detecting Glycogen in Peripheral Blood Mononuclear Cells with Periodic Acid Schiff Staining

    Published on: December 23, 2014

    Glycan Node Analysis: A Bottom-up Approach to Glycomics
    11:36

    Glycan Node Analysis: A Bottom-up Approach to Glycomics

    Published on: May 22, 2016

    Related Experiment Videos

    Last Updated: Aug 15, 2026

    Chemically-blocked Antibody Microarray for Multiplexed High-throughput Profiling of Specific Protein Glycosylation in Complex Samples
    13:21

    Chemically-blocked Antibody Microarray for Multiplexed High-throughput Profiling of Specific Protein Glycosylation in Complex Samples

    Published on: May 4, 2012

    Detecting Glycogen in Peripheral Blood Mononuclear Cells with Periodic Acid Schiff Staining
    09:42

    Detecting Glycogen in Peripheral Blood Mononuclear Cells with Periodic Acid Schiff Staining

    Published on: December 23, 2014

    Glycan Node Analysis: A Bottom-up Approach to Glycomics
    11:36

    Glycan Node Analysis: A Bottom-up Approach to Glycomics

    Published on: May 22, 2016

    Related Concept Videos

    Genome-wide Association Studies-GWAS01:11

    Genome-wide Association Studies-GWAS

    Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
    GWAS does not require the identification of the target gene involved in...
    Proteoglycans01:05

    Proteoglycans

    Glycans, a class of complex heterogeneous molecules, can be covalently attached to proteins to form glycosylated proteins that regulate various physiological and pathological processes. Glycosylated proteins or glycoproteins comprise N-linked and O-linked oligosaccharides. O-glycosylation is the most common type of protein glycosylation. Here, glycans attach to the oxygen atom of the hydroxyl groups of Serine or Threonine residues. O-linked glycosylation occurs later in protein processing,...

    Articles linked to this work by shared authors, journal, and citation graph.

    Phylogeographic review of Y chromosome haplogroups in Europe.

    International journal of legal medicine·2021

    Species identification in meat products: A new screening method based on high resolution melting analysis of cyt b gene.

    Food chemistry·2017

    Cytotoxic T lymphocyte-associated antigen 4 rs231775 polymorphism and osteosarcoma.

    Neoplasma·2017

    Two ovine mitochondrial DNAs harboring a fifth 75/76 bp repeat motif without altered gene expression in Northern Spain.

    Electrophoresis·2016

    Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing.

    International journal of laboratory hematology·2016

    Genomewide miRNA profiling of oral lichenoid disorders and oral squamous cell carcinoma.

    Oral diseases·2016

    Association between ABCB1 gene polymorphism and response to levetiracetam treatment in focal epilepsy: a prospective case-control study in a Chinese population.

    Human heredity·2026

    A frequentist test of proportional colocalization after selecting relevant genetic variants.

    Human heredity·2026

    Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

    Human heredity·2026

    Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

    Human heredity·2026

    Erratum.

    Human heredity·2026

    Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

    Human heredity·2025

    Case Report: Fabry cardiomyopathy associated with a novel truncating GLA variant, c.837_838delinsAT, p.(Gln280Ter).

    Frontiers in medicine·2026

    Three-Way Chromosomal Translocation Involving KMT2A::MLLT3 in AML: A Case Report and Genomic Characterization.

    Cytogenetic and genome research·2026

    Identification of the Novel HLA-G*01:01:39 Allele Using PolyseqOne Sequencing.

    HLA·2026

    Identification and Characterisation of a Novel HLA-DPB1*1985:01 Allele by Long-Read Sequencing.

    HLA·2026

    Splenomegaly With Thrombocytopenia: A Case of the Rare and Obvious.

    Journal of pediatric hematology/oncology·2026

    Characterisation of the Novel HLA-DPB1*1933:01 Allele by Sequencing-Based Typing.

    HLA·2026
    See all related articles
    JoVE
    x logofacebook logolinkedin logoyoutube logo
    ABOUT JoVE
    OverviewLeadershipBlogJoVE Help Center
    AUTHORS
    Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
    LIBRARIANS
    TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
    RESEARCH
    JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
    EDUCATION
    JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
    Terms & Conditions of Use
    Privacy Policy
    Policies
    Jove
    Visualize
    Contact Us