HLA-G Vectors & Virus Products | CRISPR KO, Lentivirus, AAV, Adenovirus, siRNA, ORF, cDNA, Overexpression, Knockdown and Knockout

HLA-G Expression Vectors, Lentivirus & CRISPR Knockout Vectors


Enhance your research with ready-to-use HLA-G-specific vectors and viral particles designed for reliable HLA-G overexpression, knockout, and silencing across a wide range of experimental systems. abm offers a complete portfolio of validated molecular tools – including HLA-G CRISPR knockout vectors, lentiviral particles, AAV vectors, adenovirus, ORF clones, and siRNA constructs for both in vitro and in vivo applications.


Human HLA-G Gene Overview

Gene Name major histocompatibility complex, class I, G
Gene Symbol HLA-G
Synonyms MHC-G
NCBI ID 3135
Ensembl ID ENSG00000204632
Uniprot ID P17693
Gene Type Protein coding

Gene Summary

HLA-G belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. HLA-G is expressed on fetal derived placental cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domain, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exon 6 encodes the cytoplasmic tail. [provided by RefSeq, Jul 2008]

Human HLA-G Related Products

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Mouse Gene Overview

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Gene Summary

Mouse Related Products

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Rat Gene Overview

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Gene Summary

Rat Related Products

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Accelerate Discovery with Research-Ready Constructs

Why Researchers Choose abm Workflow Benefits
Gene-Specific Constructs Eliminate time-consuming cloning and accelerate project timelines
Available as Plasmid DNA or Packaged Virus Choose delivery format that best fits your experiment
Validated Sequence Design  Ensure reliable, reproducible experimental performance
Available in Multiple Species Options  Simplify cross-species and translational research studies
Flexible Customization Services Tailor constructs with different promoters, tags, markers and other modifications 
Expert Technical Support Get guidance from gene delivery specialists

Product Overview & Key Features

System Applications Key Features
CRISPR Knockout Vectors & Viruses Targeted gene disruption & functional knockout studies •Pre-designed validated sgRNAs
•Available in All-in-One Cas9 + sgRNA or sgRNA-only formats
•Available as lentivirus, AAV and non-viral
•Ideal for stable genome editing
Lentiviral Expression Vectors & Particles Stable gene overexpression or delivery into difficult-to-transfect cells •Long-term expression through genomic integration
•Highly efficient in dividing and non-dividing cells
•Ideal for stable cell line generation
AAV Vectors & Packaged Virus In vivo delivery & transient expression with low immunogenicity •Multiple serotypes available for tissue targeting
•Excellent for animal studies and sensitive primary cells
•Episomal expression with strong safety profile
Adenovirus High-efficiency transient expression •Rapid, robust gene expression
•Large cargo capacity
•Ideal for primary cells and strong short-term expression studies
ORF Vector Template for coding sequence •Ready-to-use full-length coding sequences
•Low cost and convenient alternative to gene synthesis
siRNA Knockdown Tools Temporary gene silencing & pathway validation •Robust gene knockdown
•Ideal for target validation and preliminary functional screening 
•Available as Lentivirus, AAV or synthetic dsRNA oligos