Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all species
Show all synonyms
Select your species and application
anti-Mouse (Murine) TSPEAR Antibodies:
anti-Human TSPEAR Antibodies:
anti-Rat (Rattus) TSPEAR Antibodies:
Go to our pre-filtered search.
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