Recombinant Mouse PDE6C Protein, His (Fc)-Avi-tagged
Cat.No. : | PDE6C-6589M |
Product Overview : | Recombinant Mouse PDE6C with His (Fc)-Avi tag was expressed and purified |
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Source : | HEK293 |
Species : | Mouse |
Tag : | His&Fc&Avi |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method |
Purity : | ≥85% by SDS-PAGE |
Stability : | Stable for at least 6 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Storage : | For long term storage, aliquot and store at -20 to -80 centigrade. Avoid repeated freezing and thawing cycles. |
Storage Buffer : | PBS buffer |
Gene Name : | Pde6c phosphodiesterase 6C, cGMP specific, cone, alpha prime [ Mus musculus ] |
Official Symbol : | PDE6C |
Gene ID : | 110855 |
mRNA Refseq : | NM_001170959.1 |
Protein Refseq : | NP_001164430.1 |
UniProt ID : | Q91ZQ1 |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Customer Reviews (3)
Write a reviewTheir expertise and prompt responsiveness exemplify their dedication to providing customers with solutions and guidance.
The PDE6C protein offers exceptional quality that seamlessly aligns with my experimental requirements.
By utilizing the PDE6C protein, I can approach my research with unwavering confidence in its quality, along with the unparalleled support provided by its manufacturer.
Q&As (5)
Ask a questionWhile primarily associated with specific forms of retinal degeneration, research is ongoing to explore the broader applicability of PDE6C-targeted therapies.
PDE6C mutations can be detected through genetic testing, and early diagnosis is crucial for implementing timely interventions and potential future therapies.
Yes, genetic testing for PDE6C mutations can aid in the diagnosis of certain retinal diseases, helping to identify the underlying genetic cause.
PDE6C is primarily expressed in the retina, but low levels of expression have also been detected in certain non-ocular tissues.
Gene therapy aims to introduce functional PDE6C genes into the retina to compensate for the mutated or non-functional genes, potentially restoring normal vision.
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