Browse our anti-TSPEAR (TSPEAR) Antibodies

Full name:
anti-Thrombospondin-Type Laminin G Domain and EAR Repeats Antibodies (TSPEAR)
On www.antibodies-online.com are 36 Thrombospondin-Type Laminin G Domain and EAR Repeats (TSPEAR) Antibodies from 8 different suppliers available. Additionally we are shipping and many more products for this protein. A total of 39 TSPEAR products are currently listed.
Synonyms:
C21orf29, C330046G03Rik, DFNB98, ORF65, RGD1563108, Tnep1, TSP-EAR
list all antibodies Gene Name GeneID UniProt
TSPEAR 252974  
TSPEAR 54084 Q8WU66
TSPEAR 365546  

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Most Popular Reactivities for anti-TSPEAR (TSPEAR) Antibodies

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anti-Mouse (Murine) TSPEAR Antibodies:

anti-Human TSPEAR Antibodies:

anti-Rat (Rattus) TSPEAR Antibodies:

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Top referenced anti-TSPEAR Antibodies

  1. 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 (PubMed)
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More Antibodies against TSPEAR Interaction Partners

Mouse (Murine) Thrombospondin-Type Laminin G Domain and EAR Repeats (TSPEAR) interaction partners

  1. using a luciferase-based reporter assay, we showed that TSPEAR knock-down is associated with decreased Notch (show NOTCH1 Antibodies) signaling. In addition, NOTCH1 (show NOTCH1 Antibodies) protein expression was reduced in patient scalp skin. Moreover, TSPEAR silencing in mouse hair follicle organ cultures was found to induce apoptosis in follicular epithelial cells, resulting in decreased hair bulb diameter

  2. 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.

Human Thrombospondin-Type Laminin G Domain and EAR Repeats (TSPEAR) interaction partners

  1. using a luciferase-based reporter assay, we showed that TSPEAR knock-down is associated with decreased Notch (show NOTCH1 Antibodies) signaling. In addition, NOTCH1 (show NOTCH1 Antibodies) protein expression was reduced in patient scalp skin. Moreover, TSPEAR silencing in mouse hair follicle organ cultures was found to induce apoptosis in follicular epithelial cells, resulting in decreased hair bulb diameter

  2. TSPEAR expression is significantly downregulated in human masticatory mucosa during wound healing

  3. 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.

  4. 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.

TSPEAR Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with TSPEAR

  • thrombospondin type laminin G domain and EAR repeats (Tspear) antibody
  • thrombospondin-type laminin G domain and EAR repeats (TSPEAR) antibody
  • thrombospondin-type laminin G domain and EAR repeats (Tspear) antibody
  • C21orf29 antibody
  • C330046G03Rik antibody
  • DFNB98 antibody
  • ORF65 antibody
  • RGD1563108 antibody
  • Tnep1 antibody
  • TSP-EAR antibody

Protein level used designations for TSPEAR

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

GENE ID SPECIES
252974 Mus musculus
54084 Homo sapiens
100335468 Bos taurus
365546 Rattus norvegicus
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