兔抗TSPEAR多克隆抗体

Background:

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.

Applications:

ELISA, IHC

Name of antibody:

TSPEAR

Immunogen:

Fusion protein of human TSPEAR

Full name:

thrombospondin-type laminin G domain and EAR repeats

Synonyms：

DFNB98; TSP-EAR; C21orf29

SwissProt:

Q8WU66

ELISA Recommended dilution:

1000-5000

IHC positive control:

Human thyroid cancer and Human liver cancer

IHC Recommend dilution:

50-200