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Panoply™ Human DICER1 Knockdown Stable Cell Line

Panoply™ Human DICER1 Knockdown Stable Cell Line

Cat.No. :  CSC-DC004304

Host Cell:  HEK293 (Hela and other cell types are also available) Validation:  Real-Time RCR

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Gene Informationn

Cat. No. CSC-DC004304
Description Creative Biogene's Knockdown Cell Lines are target specific shRNA lentivirus transduced cells. The percent knockdown levels range from 75-99% depending on the gene, as evaluated by Real-Time RCR. Cells are rigorously qualified and mycoplasma free.
Gene DICER1
Host Cell HEK293 (Hela and other cell types are also available)
Host Cell Species Homo sapiens (Human)
Stability Validated for at least 10 passages
Application

(1) Studying gene functions

(2) Studying gene interactions and signaling pathways

(3) Target validation and drug discovery

(4) Designing diseases models

Quality Control Negative for bacteria, yeast, fungi and mycoplasma.
Size Form >1 × 10^6 cells / vial
Shipping Dry Ice
Storage Liquid Nitrogen
Gene Name
Gene Symbol
Synonyms
Gene Description
Gene ID
UniProt ID
mRNA Refseq
Protein Refseq
Chromosome Location
Function
Pathway
MIM
Mycoplasma Negative
Format One frozen vial containing millions of cells
Storage Liquid nitrogen
Safety Considerations

The following safety precautions should be observed.

1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum.

2. No eating, drinking or smoking while handling the stable line.

3. Wash hands after handling the stable line and before leaving the lab.

4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells.

5. All waste should be considered hazardous.

6. Dispose of all liquid waste after each experiment and treat with bleach.

Ship Dry ice
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Customer Q&As
What is DICER1 syndrome?

A: DICER1 syndrome, first reported in 1996, is a rare genetically inherited disease in which mutations in the DICER1 gene predispose the body to a variety of benign and malignant tumours

What are the clinical symptoms of DICER1 syndrome?

A: mainly multinodular goitre, pleuropneumoblastoma, cystic nephroma, Sertoli-Leydig cell tumour of the ovary, ciliary body medullary epithelioma, embryonal rhabdomyosarcoma of the uterine cervix, differentiated thyroid cancer, etc.

What is the pathogenesis of DICER1?

A: The pathogenesis is due to mutations in the DICER1 gene, which encodes a ribonucleic acid endonuclease, resulting in impaired synthesis and expression of microRNAs and the induction of tumours.

What is the genetic basis of DICER1 syndrome?

A: DICER1 syndrome is an autosomal dominant disorder in which a single mutation in one copy of the gene is sufficient to increase the risk of tumour development. Researchers reported in 2009 that DICER1 syndrome is caused by a mutation in the DICER1 gene. This is also a disease in which mutations in a gene associated with microRNA maturation cause tumours in humans.

Where is the DICER1 gene located on the gene?

A: The DICER1 gene, located on chromosome 14 at q32.13, encodes the DICER protein, a ribonucleic acid endonuclease in the RNA III family, which is directly involved in the regulation of the RNA interference (RNAi) pathway

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