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- accession：NM_007752
- 基因别名：Cp
- 基因描述：Mus musculus ceruloplasmin (Cp), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：3186
- 翻译后氨基酸长度：1061
- TranscriptVariant：This variant (2) encodes isoform b.
- 基因简介：The protein encoded by this gene is a copper-containing glycoprotein found soluble in the serum and GPI-anchored in other tissues. It oxidizes Fe(II) to Fe(III) and is proposed to play an important role in iron homeostasis. In humans mutations of this gene cause aceruloplasminemia, which is characterized by retinal degeneration, diabetes, anemia and neurological symptoms. In mouse deficiency of this gene in combination with a deficiency of its homolog hephaestin causes retinal degeneration and serves as a pathophysiological model for aceruloplasminemia and age-related macular degeneration. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jan 2013]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
