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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
A suggested positive control is mouse heart tissue lysate.
PA5-21170 can be used with blocking peptide PEP-1284.
SPRYD2, also known as Myospryn, was originally identified as the muscle-specific partner of dysbindin and as a Mef-2 target gene. It is a large scaffolding protein localized to the Z-disc/costamere region of striated muscle. SPRYD2 includes a noncanonical tripartite motif (TRIM-like) that lacks the RING domain but consists of a B-box coiled coil (BBC), fibronectin 3 (FN3) repeats, and SPRY domains. SPRYD2 interacts with desmin and calcineurin, and it has been suggested to play a role in the biogenesis of lysosome and negatively regulates slow-fiber-type transformation and skeletal muscle regeneration. SPRYD2 is dysregulated in Duchenne muscular dystrophy.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: cardiomyopathy associated 5; cardiomyopathy-associated protein 5; heart and skeletal muscle-specific and sprouty domain-containing; myospryn; stretch response protein 553; stretch-response protein 553; stretch-responsive fibronectin protein type 3; TRIM-like protein
基因别名: 2310076E16Rik; 2310076E21Rik; AA420382; AI504003; sr553; Srfsd; Tims
Entrez Gene ID: (Rat) 688915, (Mouse) 76469