ZFHX4 Rabbit Polyclonal Antibody

ZFHX4 Rabbit Polyclonal Antibody

Cat: APRab20084
Boyut:20μL Fiyat:$99_x000D_
Boyut:50μL Fiyat:$118_x000D_
Boyut:100μL Fiyat:$220_x000D_
Boyut:200μL Fiyat:$380_x000D_
Uygulama:WB,IHC,ICC/IF
Reaktivite:Human,Mouse
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:ZFHX4
Category: ポリクローナル抗体 Tags: , , , , , , , ,
ZFHX4 Rabbit Polyclonal Antibody
Konjugasyon: Unconjugated
Rabbit polyclonal Antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF
Reaktivite
Human,Mouse
Gen Adı
ZFHX4
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı ZFHX4 Rabbit Polyclonal Antibody
Açıklama Rabbit polyclonal Antibody
Konak Rabbit
Reaktivite Human,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 ZFHX4
Alternatif İsimler
Gen Kimliği 79776
SwissProt Kimliği Q86UP3
İmmünojen Synthesized peptide derived from part region of human protein
Uygulama
Uygulama WB,IHC,ICC/IF
Seyreltme Oranı WB 1:500-1:1000,IHC 1:200-1:500,ICC/IF 1:50-1:200
Moleküler Ağırlık 392kDa
Araştırma Alanı
Epigenetics and Nuclear Signaling; Transcription; Domain Families; Zinc Finger; Developmental Families
Arka Plan
disease:A chromosomal aberration involving [ZFHX4] is found in one patient with ptosis. Translocation t(1;8)(p34.3;q21.12).,function:May play a role in neural and muscle differentiation (By similarity). May be involved in transcriptional regulation.,similarity:Belongs to the krueppel C2H2-type zinc-finger protein family.,similarity:Contains 20 C2H2-type zinc fingers.,similarity:Contains 4 homeobox DNA-binding domains.,tissue specificity:Expressed in brain, skeletal muscle and liver. Very low expression in stomach.,disease:A chromosomal aberration involving [ZFHX4] is found in one patient with ptosis. Translocation t(1;8)(p34.3;q21.12).,function:May play a role in neural and muscle differentiation (By similarity). May be involved in transcriptional regulation.,similarity:Belongs to the krueppel C2H2-type zinc-finger protein family.,similarity:Contains 20 C2H2-type zinc fingers.,similarity:Contains 4 homeobox DNA-binding domains.,tissue specificity:Expressed in brain, skeletal muscle and liver. Very low expression in stomach.,
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