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C1orf21 Knockout HK-2 Cell Line

Cat. No. ARG43762
Product Type:

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Short Description

The C1orf21 Knockout HK-2 Cell Line is a CRISPR/Cas9-edited human kidney proximal tubule epithelial model with targeted disruption of C1orf21, an uncharacterized gene encoding a predicted DNA-binding protein linked to RNA Polymerase I transcription. This stable knockout line enables investigation of C1orf21??s role in transcriptional regulation and its potential interaction with Pol I subunits. It supports studies in renal physiology, chromosome 1p36 deletion syndrome, and cancer. Applications include transcriptomic profiling, validation by RT-qPCR, protein analysis, and cell-based assays for nephrotoxicity and viability.

Product Details
Cell Engineering
Immortalization
Culture Conditions
Quality Control
Disclaimer

Product Details

Cell Engineering Information

Gene Name:
C1orf21
Gene Identifier:
NCBI Gene ID 81563

Immortalization Information

Culture Conditions

Temperature:
37°C
Atmosphere:
5% CO₂

Quality Control

Sterility testing:
The bacterial, yeast, and fungi are not detected in these cells by daily monitor.

Disclaimer

Intended Use:
This product is intended for laboratory in vitro use only. It is not intended for diagnostic, therapeutic, or clinical applications.
Disclaimer:
Ascent Research endeavors to provide accurate and up-to-date product information. However, no warranties or representations are made regarding its completeness or reliability.
Usage:
By accepting this product, the customer acknowledges and agrees to assume all risks associated with its receipt, handling, storage, disposal, and use. This product is provided "AS IS".

Description

The C1orf21 Knockout HK-2 Cell Line is a precisely engineered human cellular model in which the C1orf21 gene is disrupted via CRISPR/Cas9-mediated editing. Based on the well-characterized HK-2 immortalized kidney proximal tubule epithelial cell line, this product offers a stable loss-of-function tool for interrogating the biological roles of C1orf21. The knockout is achieved through targeted genome modification, generating a permanent alteration that abrogates gene function. Researchers can thus bypass the variability and transient effects inherent to RNA interference methods.

HK-2 cells retain core features of proximal tubule epithelium, including polarized structure, expression of brush border enzymes, and active transport of solutes. They also perform metabolic transformations and endocrine functions typical of this nephron segment. As a result, HK-2 is extensively used to model renal physiology, toxicology, and disease states such as acute kidney injury, fibrosis, and drug-induced nephrotoxicity. Its robust culture characteristics and amenability to genetic manipulation make it an optimal chassis for gene-editing studies.

The C1orf21 protein is predicted to contain DNA-binding domains, implicating it in transcriptional regulation. It is associated with RNA Polymerase I transcription pathways and may engage subunits of the Pol I complex, although its precise interactome and downstream effects are not known. By using C1orf21 knockout cells, scientists can begin to map this uncharacterized factor??s involvement in Pol I-dependent rRNA synthesis and global gene expression control. The model enables identification of transcriptional targets and signaling partners that mediate C1orf21??s cellular functions.

In the renal proximal tubule context, loss of C1orf21 may impact programs governing solute reabsorption, metabolism, and endocrine activity. This line is especially valuable for studying chromosome 1p36 deletion syndrome, which can involve renal anomalies, and for cancer research given the gene??s location in a frequently altered region. The model facilitates dissection of how C1orf21 contributes to transcriptional homeostasis in highly active epithelia, with implications for understanding both normal kidney physiology and neoplastic transformation.

Key applications include transcriptome-wide RNA-seq analysis to reveal pathways altered by C1orf21 knockout, RT-qPCR for validation, and western blotting or immunocytochemistry to examine protein expression and localization when reagents permit. Cell viability and apoptosis assays can assess the gene??s role in stress responses. The line is suitable for drug toxicity testing and disease modeling. For further details, including bulk orders, please contact Ascent Research.