人 FGB (NM_001184741) cDNA克隆

Accession: NM_001184741
基因名称: FGB
基因描述: Homo sapiens fibrinogen beta chain (FGB), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1299 (查看编码区序列)
翻译后氨基酸长度: 432 (查看氨基酸序列)
Transcript Variant: This variant (2) uses an alternate in-frame splice site in the coding region, compared to variant 1. This results in a shorter protein (isoform 2), compared to isoform 1.
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G123327 人 FGB (NM_001184741) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including afibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia and thrombotic tendency. [provided by RefSeq, Jul 2008]