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Panoply™ Human ATG7 Knockdown Stable Cell Line

Panoply™ Human ATG7 Knockdown Stable Cell Line

Cat.No. :  CSC-DC001106

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

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Gene Informationn

Cat. No. CSC-DC001106
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 ATG7
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 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.

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Customer Q&As
What is the role of ATG7 in autophagy?

A: ATG7 encodes a ubiquitin E1-like ligase that activates ATG12 prior to its binding to ATG5, promoting the expansion of prophagosomes.

What is the relationship between ATG7 and LC3-I and LC3-II?

A:  ATG7 promotes the lipidation of the protein LC3-I with phosphatidylethanolamine to produce LC3-II, which is found on the inner and outer autophagosome membranes and recruits cytoplasmic cargo into autophagosomes either directly or via selective bridging proteins.

What is the relationship between mild myopathy and autophagy in ATG7-deficient human skeletal muscle?

A: ATG7 mutations cause congenital neurodevelopmental disorders due to impaired autophagy, reinforcing the association of ATG gene mutations in the autophagic system with congenital neurodevelopmental disorders

What are the characteristics of patients with mutations in the ATG7 gene?

A: Autosomal recessive, all patients present with a neurodevelopmental syndrome characterized by cerebellar hypoplasia, posterior corpus callosum thinning, ataxia, developmental delay, musculoskeletal abnormalities and facial dysmorphism

What is the biological function of ATG7?

A: An important example is ATG7, an essential autophagy effector enzyme that in concert with other ATG proteins, also regulates immunity, cell death and protein secretion, and independently regulates the cell cycle and apoptosis.

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