储存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆号: PT0363R
特异性: Endogenous
基因名称: FTH1
蛋白名称: Ferritin heavy chain
别名: FTH1;FTH;FTHL6;OK/SW-cl.84;PIG15;Ferritin heavy chain;Ferritin H subunit;Cell proliferation-inducing gene 15 protein
Organism-1: Human
基因ID-1: 2495
SwissProt-1: P02794
Organism-2: Mouse
基因ID-2: 14319
SwissProt-2: P09528
Organism-3: Rat
基因ID-3: 25319
SwissProt-3: P19132
背景: This gene encodes the heavy subunit of ferritin, the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined. [provided by RefSeq, Jul 2008],
储存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆号: PT0363R
特异性: Endogenous
基因名称: FTH1
蛋白名称: Ferritin heavy chain
别名: FTH1;FTH;FTHL6;OK/SW-cl.84;PIG15;Ferritin heavy chain;Ferritin H subunit;Cell proliferation-inducing gene 15 protein
Organism-1: Human
基因ID-1: 2495
SwissProt-1: P02794
Organism-2: Mouse
基因ID-2: 14319
SwissProt-2: P09528
Organism-3: Rat
基因ID-3: 25319
SwissProt-3: P19132
背景: This gene encodes the heavy subunit of ferritin, the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative diseases. This gene has multiple pseudogenes. Several alternatively spliced transcript variants have been observed, but their biological validity has not been determined. [provided by RefSeq, Jul 2008],