68kDa Neurofilament Rabbit Monoclonal Antibody

68kDa Neurofilament Rabbit Monoclonal Antibody

Cat: AMRe86922
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC/IF,IP
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:68kDa Neurofilament
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , ,
68kDa Neurofilament Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF,IP
Reaktivite
Human,Mouse,Rat
Gen Adı
68kDa Neurofilament
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı 68kDa Neurofilament 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 68kDa Neurofilament
Alternatif İsimler NFL; NF-L; NF68; CMT1F; CMT2E; PPP1R110
Gen Kimliği 4747,18039,83613
SwissProt Kimliği P08551,P08551,P19527
İmmünojen Recombinant protein of mouse 68kDa Neurofilament
Uygulama
Uygulama WB,IHC,ICC/IF,IP
Seyreltme Oranı WB 1:500-1:2000,IHC 1:500-1:2000,ICC/IF 1:20-1:50,IP 1:20-1:50
Moleküler Ağırlık Calculated MW:62 kDa; Observed MW:68 kDa
Araştırma Alanı
Arka Plan
Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the light chain neurofilament protein. Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E), disorders of the peripheral nervous system that are characterized by distinct neuropathies. A pseudogene has been identified on chromosome Y. [provided by RefSeq, Oct 2008]
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