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The antibody detects endogenous levels of total TSPEAR protein.
This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012].
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: protein TSPEAR; Thrombospondin-type laminin G domain and EAR repeat-containing protein; thrombospondin-type laminin G domain and EAR repeats; thrombospondin-type laminin G domain and EAR repeats-containing protein; TSP-EAR
基因别名: C21orf29; DFNB98; TSP-EAR; TSPEAR
UniProt ID: (Human) Q8WU66
Entrez Gene ID: (Human) 54084
分子生物学功能: intercellular signal molecule