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Human HDAC3 adenoviral particles

Human HDAC3 adenoviral particles

Cat.No. :  AD00183Z

Titer: ≥1x10^10 IFU/mL / ≥1x10^11 IFU/mL / ≥1x10^11 VP/mL / ≥1x10^12 VP/mL Size: 100 ul/500 ul/1 mL

Storage:  -80℃ Shipping:  Frozen on dry ice

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Adenovirus Particle Information

Quality Control

Gene Informationn

Cat. No. AD00183Z
Target Gene HDAC3
Species Human
Product Type Adenoviral particle
Insert HDAC3
Titer Varies lot by lot, for example, ≥1x10^10 IFU/mL, ≥1x10^11 IFU/mL, ≥1x10^11 VP/mL etc.
Size Varies lot by lot, for example, 250 ul, 500 ul, 1 mL etc.
Storage Store at -80℃. Avoid multiple freeze/thaw cycles.
Shipping Frozen on dry ice
Creative Biogene ensures high-quality adenovirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between adenovirus particle lots.
Endotoxin Endotoxins, primarily derived from Gram-negative bacteria, can trigger adverse immune responses. Endotoxin contamination is a significant concern in adenovirus production, especially for applications in animal studies and gene therapy. Creative Biogene utilizes rigorous endotoxin detection methods to monitor the endotoxin level in our produced adenovirus particles to ensure regulatory compliance.
Sterility Creative Biogene ensures that adenovirus products are free of any bacterial, fungal and other microbial contamination.
Ad5 E1 Detection All Creative Biogene adenoviruses are PCR tested to ensure that there are no detectable E1 sequences in the particles, which could be from revertants or external E1 contamination.
RCA Assays Adenovirus products originating at Creative Biogene are guaranteed to have undetectable replication-competent adenovirus (RCA). This quality control measure is important because there is always the possibility of wild-type contamination due to revertants or environmental sources.
PFU Titering All purified adenovirus preparations are tested for infectious titer. Creative Biogene's PFU test takes a few days longer but counts true plaques in HEK cells rather than estimating PFU titers via IHC staining or TCI50 of infected cells.
Gene Name
Gene Symbol
Synonyms
Gene Description
Gene ID
UniProt ID
mRNA Refseq
Protein Refseq
Chromosome Location
Function
Pathway
MIM
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Histone deacetylase 3 (HDAC3) is a key member of the histone deacetylase family and plays a critical role in epigenetic regulation by removing acetyl groups from histones and non-histone proteins. The enzymatic activity of HDAC3 regulates chromatin structure and gene expression, affecting multiple cellular processes such as proliferation, differentiation, apoptosis, and metabolic homeostasis. HDAC3 is unique among class I HDACs in that it plays an important role in embryonic development and is involved in a variety of physiological and pathological states including cancer, neurodegenerative diseases, and metabolic disorders. It is a core component of multiprotein complexes such as nuclear receptor co-repressors (NCoRs) and silencing mediators of retinoic acid and thyroid hormone receptors (SMRTs), which are essential for its recruitment to target genes and exerting regulatory specificity. Dysregulation of HDAC3 is associated with a variety of diseases, making it a promising therapeutic target for drug development.

Human HDAC3 Adenoviral Particles are high-titer, replication-defective viral vectors designed to deliver the HDAC3 gene to mammalian cells for functional studies or therapeutic applications. These particles are based on adenovirus serotype 5 (Ad5) and achieve high transduction efficiencies in a variety of cell types, including primary cells and difficult-to-transfect cells. The episomal nature of adenoviral particles avoids the risk of genomic integration and is ideal for short-term overexpression studies. They are widely used in fields such as cancer biology, neurobiology, and metabolic research to investigate the role of HDAC3 in gene regulation, cell signaling, and disease mechanisms.
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Customer Reviews
Consistent Performance

I’ve used multiple batches of HDAC3 adenoviral particles, and each one has delivered consistent, high-quality results. The transduction efficiency is excellent, even in difficult cell types.

Germany

06/21/2025

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