DLX3 Rabbit Monoclonal Antibody

DLX3 Rabbit Monoclonal Antibody

Cat: AMRe02972
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Boyut:200μL Fiyat:$520_x000D_
Uygulama:WB
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:DLX3
Category: 組換えモノクローナル抗体 Tags: , , , , ,
DLX3 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB
Reaktivite
Human
Gen Adı
DLX3
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı DLX3 Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human
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 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% protective protein
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı DLX3
Alternatif İsimler AI4; TDO
Gen Kimliği 1747
SwissProt Kimliği O60479
İmmünojen A synthetic peptide of human DLX3
Uygulama
Uygulama WB
Seyreltme Oranı WB 1:500-1:1000
Moleküler Ağırlık Calculated MW: 32 kDa; Observed MW: 32 kDa
Araştırma Alanı
Epigenetics and Nuclear Signaling
Arka Plan
Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.
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