Home / RNASEH1 Knockout Cell Lines

RNASEH1 Knockout Cell Lines

Gene: RNASEH1

Official Full Name: ribonuclease H1provided by HGNC

Gene Summary: This gene encodes an endonuclease that specifically degrades the RNA of RNA-DNA hybrids and plays a key role in DNA replication and repair. Alternate in-frame start codon initiation results in the production of alternate isoforms that are directed to the mitochondria or to the nucleus. The production of the mitochondrial isoform is modulated by an upstream open reading frame (uORF). Mutations in this gene have been found in individuals with progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2. Alternative splicing results in additional coding and non-coding transcript variants. Pseudogenes of this gene have been defined on chromosomes 2 and 17. [provided by RefSeq, Jul 2017]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO21487 RNASEH1 Knockout cell line (HeLa) Human RNASEH1 1:3~1:6 Negative Online Inquiry
KO21488 RNASEH1 Knockout cell line (HCT 116) Human RNASEH1 1:2~1:4 Negative Online Inquiry
KO21489 RNASEH1 Knockout cell line (HEK293) Human RNASEH1 1:3~1:6 Negative Online Inquiry
KO21490 RNASEH1 Knockout cell line (A549) Human RNASEH1 1:3~1:4 Negative Online Inquiry

Background

RNASEH1 Gene Knockout Cell Lines are specialized cell models in which the RNASEH1 gene has been selectively inactivated or "knocked out," resulting in the absence of RNase H1 enzyme activity. This enzyme plays a crucial role in RNA metabolism by degrading RNA strands that are hybridized to DNA, thereby participating in processes related to DNA replication and repair, as well as RNA degradation. By disrupting the RNASEH1 gene, these cell lines allow researchers to study the physiological and pathological impacts of RNase H1 deficiency, as well as to elucidate the molecular mechanisms underlying RNA-DNA hybrid dynamics.

The functionality of the RNASEH1 Gene Knockout Cell Lines lies in their ability to simulate specific cellular contexts that reflect RNase H1 deficiency. Researchers employing these models can investigate how disrupted RNA processing affects cellular functions, gene expression, and the overall molecular environment, which can have implications for understanding diseases such as cancer, neurodegenerative disorders, and viral infections. Additionally, these cell lines pave the way for exploring therapeutic strategies aimed at restoring normal function or compensating for the absence of RNase H1.

Scientifically, RNASEH1 Gene Knockout Cell Lines represent significant tools in both basic and applied research. Their specific application in studying cellular responses to stress, DNA damage repair pathways, and therapeutic drug interactions provides unparalleled insights into RNA biology and genetic regulation.

Compared to traditional cell lines, these knockout models offer unique advantages, including higher specificity and relevance in studies of health and disease states associated with RNA metabolism. Furthermore, they provide a direct platform for testing novel drugs or treatments targeting RNase H1 functions or related pathways.

For researchers and clinicians, the value of RNASEH1 Gene Knockout Cell Lines lies in their ability to advance scientific understanding and therapeutic innovation in rapidly evolving fields. With a rich portfolio of biological products and an extensive background in cellular genomics, our company is committed to providing high-quality models that empower scientific discovery and facilitate advancements in personalized medicine.

Please note that all services are for research use only. Not intended for any clinical use.

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.

0

There is no product in your cart.