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Bottles, spin columns, filter plates, and complete purification kits containing Proteins L, A, A/G, or G immobilized on crosslinked, beaded affinity resins of various material compositions. Ideal for antibody purification and immunoprecipitation applications.
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The protein encoded by this gene belongs to the albumin gene family It is a multifunctional protein found in plasma ascitic fluid cerebrospinal fluid and on the surface of many cell types It binds to vitamin D and its plasma metabolites and transports them to target tissues Alternatively spliced transcript variants encoding different isoforms have been found for this gene
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
The protein encoded by this gene belongs to the albumin gene family It is a multifunctional protein found in plasma ascitic fluid cerebrospinal fluid and on the surface of many cell types It binds to vitamin D and its plasma metabolites and transports them to target tissues Alternatively spliced transcript variants encoding different isoforms have been found for this gene
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Protein. Full-length NAPRTase Bacillus subtilis. Source E. coli. Endotoxin content N/A. Liquid. in 20mM TRIS-HCl, pH 7.8 containing 50mM sodium chloride. Purity >98% SDS-PAGE. Nicotinate Phosphoribosyltransferase NAPRTase is involved in the biological processes of pyridine nucleotide biosynthesis and nicotinate nucleotide salvage and functions by catalyzing the conversion of nicotinic acid NA to NA mononucleotide NaMN. It is a crucial factor in the NAD biosynthesis pathway. Catalytic activity Beta-nicotinate D-ribonucleotide diphosphate = nicotinate 5-phospho-alpha-D-ribose 1-diphosphate.
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Recombinant protein. Mouse FGF-23 aa25-251 is fused at the C-terminus to the Fc portion of human IgG1. Activates ERK and FRS2alpha phosphorylation in Klotho expressing cells. Source/Host HEK 293 cells. Purity >90% SDS-PAGE. Lyophilized. Contains PBS. FGF-23 Fibroblast growth factor 23 is a regulator of phosphate homeostasis. It upregulates EGR1 expression in the presence of KLBy. Acts directly on the parathyroid to decrease PTH secretion. Regulates the vitamin-D metabolism. Negatively regulates osteoblast differentiation and matrix mineralization. Defects in FGF-23 are the cause of autosomal dominant hypophosphataemic rickets ADHR and of hyperphosphatemic familial tumoral calcinosis HFTC.
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Protein. Signal peptide and human FGF-23 aa 1-251 are fused at the C-terminus to the Fc portion of human IgG1. Source HEK 293 cells. Endotoxin content <0.1EU/µg purified protein LAL test Lonza. Liquid. 0.2µm-filtered solution in PBS. Purity >90% SDS-PAGE. FGF-23 Fibroblast growth factor 23 is a regulator of phosphate homeostasis. It upregulates EGR1 expression in the presence of KLBy. Acts directly on the parathyroid to decrease PTH secretion. Regulates the vitamin-D metabolism. Negatively regulates osteoblast differentiation and matrix mineralization. Defects in FGF-23 are the cause of autosomal dominant hypophosphataemic rickets ADHR and of hyperphosphatemic familial tumoral calcinosis HFTC.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Protein. Signal peptide and human FGF-23 aa 1-251 are fused at the C-terminus to the Fc portion of human IgG1. Source HEK 293 cells. Endotoxin content <0.1EU/µg purified protein LAL test Lonza. Liquid. 0.2µm-filtered solution in PBS. Purity >90% SDS-PAGE. FGF-23 Fibroblast growth factor 23 is a regulator of phosphate homeostasis. It upregulates EGR1 expression in the presence of KLBy. Acts directly on the parathyroid to decrease PTH secretion. Regulates the vitamin-D metabolism. Negatively regulates osteoblast differentiation and matrix mineralization. Defects in FGF-23 are the cause of autosomal dominant hypophosphataemic rickets ADHR and of hyperphosphatemic familial tumoral calcinosis HFTC.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More