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TSPEAR encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). Additionally we are shipping and many more products for this protein.
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Human Polyclonal TSPEAR Primary Antibody for FACS, IHC (p) - ABIN653223
Scheel, Tomiuk, Hofmann: A common protein interaction domain links two recently identified epilepsy genes. in Human molecular genetics 2002
Show all 2 references for ABIN653223
TSPEAR, cause disorders with auditory features: epilepsy, which can include auditory features in humans; audiogenic seizures in animals; and/or hearing impairments in humans and mice.
TSPEAR expression is significantly downregulated in human masticatory mucosa during wound healing
The TSPEAR/C21orf29 promoter is activated by Trichostatin A (TSA (show PRDX2 Antibodies)) treatment according to promoter reporter assays in HEK (show EPHA3 Antibodies) 293 cells.
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.
thrombospondin N-terminal domain/EPTP protein 1
, thrombospondin-type laminin G domain and EAR repeat-containing protein
, thrombospondin-type laminin G domain and EAR repeats protein
, protein TSPEAR
, thrombospondin-type laminin G domain and EAR repeats-containing protein