Gene: PYGM
Official Full Name: glycogen phosphorylase, muscle associatedprovided by HGNC
Gene Summary: This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA13991 | PYGM Knockout cell line (AC16) | Human | PYGM | 1:3-1:4 | negative | Online Inquiry |
| KOA29434 | PYGM Knockout cell line (BEAS-2B) | Human | PYGM | 1:3~1:4 | negative | Online Inquiry |
| KOA44864 | PYGM Knockout cell line (U-2932) | Human | PYGM | 1:2-1:4 | negative | Online Inquiry |
| KOA60248 | PYGM Knockout cell line (TPC-1) | Human | PYGM | 1:5-1:8 | negative | Online Inquiry |
| KOA75673 | PYGM Knockout cell line (NCM460) | Human | PYGM | 1:2~1:3 | negative | Online Inquiry |
Please note that all services are for research use only. Not intended for any clinical use.
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.
|
There is no product in your cart. |
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.