PHOX2A Rabbit Monoclonal Antibody

PHOX2A Rabbit Monoclonal Antibody

Cat: AMRe86388
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,ICC/IF
Reaktivite:Human,Mouse
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:PHOX2A
Category: 組換えモノクローナル抗体 Tags: , , , , , ,
PHOX2A Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,ICC/IF
Reaktivite
Human,Mouse
Gen Adı
PHOX2A
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı PHOX2A Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse
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 PHOX2A
Alternatif İsimler ARIX; FEOM2; NCAM2; PMX2A; CFEOM2
Gen Kimliği 401
SwissProt Kimliği O14813
İmmünojen A synthetic peptide of human PHOX2A
Uygulama
Uygulama WB,ICC/IF
Seyreltme Oranı WB 1:1000-1:5000,ICC/IF 1:100-1:200
Moleküler Ağırlık Calculated MW:30 kDa; Observed MW:36-38 kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system. It regulates the expression of tyrosine hydroxylase and dopamine beta-hydroxylase, two catecholaminergic biosynthetic enzymes essential for the differentiation and maintenance of the noradrenergic neurotransmitter phenotype. The encoded protein has also been shown to regulate transcription of the alpha3 nicotinic acetylcholine receptor gene. Mutations in this gene have been associated with autosomal recessive congenital fibrosis of the extraocular muscles. [provided by RefSeq, Jul 2008]
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