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Paternally expressed gene 10 protein
It is accepted that an HbA1c of >6
Desmin-related myofibrillar myopathy (DRM or desminopathy) is a subgroup of the myofibrillar myopathy diseases and is the result of a mutation in the gene that codes for desmin which by changing the protein structure prevents it from forming protein filaments
application dilution species WB 1:1000 null IHC-P 1:2000 null
FGFR2b Recombinant Rabbit mAb (SDT-423-2) Viral Protein Paternally expressed gene 10 proteinProduct Specification Host Rabbit Antigen FGFR2b Synonyms FGFR2IIIb, Fibroblast growth factor receptor 2b, Fibroblast growth factor receptor 2IIIb Immunogen Synthetic Peptide Location Secreted, Cell membrane Accession P21802 3 Clone Number SDT 423 2 Antibody Type Recombinant mAb Application WB, IHC P, FCM Reactivity Hu Purification Protein A Concentration 0. 5 mg ml Conjugation Unconjugated Physical Appearance Liquid Storage Buffer PBS, 40% Glycerol,
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