UTRO Rabbit Polyclonal Antibody

UTRO Rabbit Polyclonal Antibody

Cat: APRab19695
Boyut:20μL Fiyat:$99_x000D_
Boyut:50μL Fiyat:$118_x000D_
Boyut:100μL Fiyat:$220_x000D_
Boyut:200μL Fiyat:$380_x000D_
Uygulama:IHC,ICC/IF
Reaktivite:Human,Rat,Mouse
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:UTRN
Category: ポリクローナル抗体 Tags: , , , , , , ,
UTRO Rabbit Polyclonal Antibody
Konjugasyon: Unconjugated
Rabbit polyclonal Antibody
Uygulama
IHC  ICC/IF  ELISA IHC,ICC/IF
Reaktivite
Human,Rat,Mouse
Gen Adı
UTRN
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı UTRO Rabbit Polyclonal Antibody
Açıklama Rabbit polyclonal Antibody
Konak Rabbit
Reaktivite Human,Rat,Mouse
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
Klonalite Polyclonal
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Saflaştırma Affinity purification
Antijen Bilgisi
Gen Adı UTRN
Alternatif İsimler DMDL DRP1
Gen Kimliği 7402
SwissProt Kimliği P46939
İmmünojen Synthesized peptide derived from part region of human protein
Uygulama
Uygulama IHC,ICC/IF
Seyreltme Oranı IHC 1:50-1:300,ICC/IF 1:50-1:200
Moleküler Ağırlık 377kDa
Araştırma Alanı
Arka Plan
This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008],function:May play a role in anchoring the cytoskeleton to the plasma membrane.,online information:Utrophin entry,similarity:Contains 1 WW domain.,similarity:Contains 1 ZZ-type zinc finger.,similarity:Contains 2 CH (calponin-homology) domains.,similarity:Contains 20 spectrin repeats.,subcellular location:Neuromuscular junction.,subunit:Interacts with the syntrophins SNTA1; SNTB1 and SNTB2. Interacts with SYNM.,tissue specificity:Muscle.,
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