MECP2 Mouse Monoclonal Antibody

MECP2 Mouse Monoclonal Antibody

Cat: AMM81579
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC,ELISA,FC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:MECP2
Category: マウスモノクローナル抗体 Tags: , , , , , , , ,
MECP2 Mouse Monoclonal Antibody
Konjugasyon: Unconjugated
Mouse monoclonal Antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC,ELISA,FC
Reaktivite
Human
Gen Adı
MECP2
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı MECP2 Mouse Monoclonal Antibody
Açıklama Mouse monoclonal Antibody
Konak Mouse
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip Mouse IgG1
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 Purified antibody in PBS with 0.05% sodium azide
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı MECP2
Alternatif İsimler RS; RTS; RTT; PPMX; MRX16; MRX79; MRXSL; AUTSX3; MRXS13
Gen Kimliği 4204
SwissProt Kimliği P51608
İmmünojen Purified recombinant fragment of human MECP2 (AA: 7-148) expressed in E. Coli.
Uygulama
Uygulama WB,IHC,ICC,ELISA,FC
Seyreltme Oranı WB 1:500-1:2000,IHC 1:200-1:1000,ICC 1:200-1:1000,ELISA 1:5000-1:20000,FC 1:200-1:400
Moleküler Ağırlık 52.4kDa
Araştırma Alanı
Arka Plan
DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females.
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