Human GYS1 Knockdown Cell Lysate

• Cat.No.: GYS1-193HKCL
• Product Overview: WB-validated GYS1 Knockdown HeLa Cell Lysate

Specification

• Species: Human
• Source: HeLa
• Tag: Non
• Description: The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
• Form: Cell-Tissue Lysis buffer
• Molecular Mass: 84 kDa
• Notes: Instruction of use: This knockdown cell lysate should be paired with wild-type HeLa cell lysate for use. For Western blotting, we recommend running wild-type and knockdown lysates on the same gel, and loading each well with equal volume and equal amount of total proteins.
• Storage: Store at -20 centigrade for two years.
• Concentration: Lot-specific
• Shipping: Blue Ice
• Components: 1 vial of 100 μg WT HeLa cell lysate 1 vial of 100 μg GYS1 KD HeLa cell lysate
• Protein Pathways: Insulin signaling pathway, Starch and sucrose metabolism
• Lysate QC: RT-qPCR; Western Blotting (WB)

Gene Information

• Gene Name: GYS1 glycogen synthase 1 (muscle) [ Homo sapiens (human) ]
• Official Symbol: GYS1
• Synonyms: GYS1; glycogen synthase 1 (muscle); GYS; glycogen [starch] synthase, muscle; GSY
• Gene ID: 2997
• mRNA Refseq: NM_001161587
• Protein Refseq: NP_001155059
• MIM: 138570
• UniProt ID: P13807