Oligodendrocyte Specific Protein Rabbit Monoclonal Antibody

Oligodendrocyte Specific Protein Rabbit Monoclonal Antibody

Cat: AMRe87217
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,FC
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Oligodendrocyte Specific Protein
Category: 組換えモノクローナル抗体 Tags: , , , , , , ,
Oligodendrocyte Specific Protein Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,FC
Reaktivite
Human,Mouse,Rat
Gen Adı
Oligodendrocyte Specific Protein
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Oligodendrocyte Specific Protein Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse,Rat
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
Klonalite Monoclonal
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı Oligodendrocyte Specific Protein
Alternatif İsimler OSP; OTM
Gen Kimliği 5010
SwissProt Kimliği O75508
İmmünojen A synthetic peptide of human Oligodendrocyte Specific Protein
Uygulama
Uygulama WB,FC
Seyreltme Oranı WB 1:1000-1:5000,FC 1:100-1:500
Moleküler Ağırlık Calculated MW:22 kDa; Observed MW:22 kDa
Araştırma Alanı
Arka Plan
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]
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