The novel HLA-C*03:04:99 allele, identified by sanger dideoxy nucleotide sequencing in a Chinese individual

Related Experiment Video

Updated: Sep 2, 2025

Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix
10:37

Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix

Published on: October 20, 2021

3.0K

Guang-Cui He1, Zhong-Zheng Zheng2, Ke-Ming Du2

  • 1Department of Hematology, The General Hospital of Western Theater Command, PLA, Chengdu, China.

HLA
|August 9, 2022
PubMed

Abstract:

HLA-C*03:04:99 differs from HLA-C*03:04:01:01 by one nucleotide in exon 5.

Keywords:
HLA-C*03:04:99novel allelesequencing-based typing

More Related Videos

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment

Published on: July 18, 2017

11.9K
Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
08:07

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation

Published on: September 6, 2017

10.2K

Related Experiment Videos

Last Updated: Sep 2, 2025

Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix
10:37

Analysis of HBV-Specific CD4 T-cell Responses and Identification of HLA-DR-Restricted CD4 T-Cell Epitopes Based on a Peptide Matrix

Published on: October 20, 2021

3.0K
High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment

Published on: July 18, 2017

11.9K
Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
08:07

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation

Published on: September 6, 2017

10.2K

Related Concept Videos

Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

15.7K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.7K

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

Novel highly selective ROCK2 inhibitor (TDI01) for the treatment of chronic graft-versus-host disease: a multicenter, open-label phase Ib/II study.

Signal transduction and targeted therapy·2026

Incidence and risk factors for graft failure after allogeneic hematopoietic stem cell transplantation in patients with myelofibrosis.

Bone marrow transplantation·2025

Glucose starvation mimetic aldometanib removes immune barriers permitting mice with hepatocellular carcinoma to live to normal ages.

Cell research·2025

An innovative full-size pathogenic tandem duplication mutation precise detection system based on next-generation sequencing.

Experimental biology and medicine (Maywood, N.J.)·2025

Triple stem cell infusion alleviated graft-versus-host disease and improves outcomes in unmanipulated haploidentical hematopoietic stem cell transplantation.

Cell transplantation·2025

Identification of the Novel HLA-A*24:649 Allele by Next-Generation Sequencing in a Chinese Individual.

HLA·2025

The Novel HLA-C*01:309 Allele, Identified by Sanger Dideoxy Nucleotide Sequencing in a Chinese Individual.

HLA·2026

Identification of a Novel HLA-G Allele, HLA-G*01:65, Using PolyseqOne and Oxford Nanopore Sequencing.

HLA·2026

Identification of the Novel HLA-B*35:670 Allele by Next-Generation Sequencing in a Bone Marrow Donor.

HLA·2026

Functional Assessment of HLA-E Promoter and 3' UTR Polymorphisms.

HLA·2026

The Full Genomic Sequence of the HLA-DRB1*15:140 Allele Identified Using PacBio Sequencing.

HLA·2026

AminoAcid3D: An Algorithm for Designing HLA Single Antigen Panels and Predicting the Essential Regions of Epitopes Based on Antibody Reactivity Profiles.

HLA·2026

Bazex-Dupré-Christol Syndrome Without Basal Cell Carcinoma Associated With a Large Interstitial Duplication at Xq26.1.

Genes, chromosomes & cancer·2026

Very Low Frequency of SCA27B Among Undiagnosed Cerebellar Ataxia Patients in Peru.

Cerebellum (London, England)·2026

A Case of Autosomal Dominant Alport Syndrome with Normal Type IV Collagen α5 Staining Diagnosed by a Genetic Analysis.

Internal medicine (Tokyo, Japan)·2026

Characterisation of the Novel HLA-DQB1*03:567 and HLA-DQB1*03:613 Alleles by Next-Generation Sequencing.

HLA·2026

Molecular Characterisation of the Novel HLA-A*30:272 Allele Identified by Third-Generation Sequencing.

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