TSPEAR 抗体
(Thrombospondin-Type Laminin G Domain and EAR Repeats (TSPEAR))
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].
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TSPEAR 抗体
High quality antibodies with extensive validation data.
Recommended TSPEAR 抗体
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Reactivity
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Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
WB, FACS, IHC (p)
Validations
- (1)
- (3)
Cat. No.
ABIN653223
Quantity
400 μL
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, IHC
Validations
- (2)
Cat. No.
ABIN7240748
Quantity
200 μL
Datasheet
Datasheet
Reactivity
Human
Application
WB, FACS, IHC (p), EIA
Validations
- (3)
Cat. No.
ABIN950880
Quantity
0.4 mL
Datasheet
Datasheet
Latest Publications for our TSPEAR Products
: "Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness." in: Human molecular genetics, Vol. 21, Issue 17, pp. 3835-44, (2012) (PubMed).Synonyms and alternative names related to TSPEAR
thrombospondin type laminin G domain and EAR repeats (Tspear), thrombospondin type laminin G domain and EAR repeats (TSPEAR), thrombospondin-type laminin G domain and EAR repeats (Tspear), C21orf29, C330046G03Rik, DFNB98, ORF65, RGD1563108, Tnep1, TSP-EARProtein 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
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