Argininosuccinate Lyase Rabbit Monoclonal Antibody

Argininosuccinate Lyase Rabbit Monoclonal Antibody

Cat: AMRe86221
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IP
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Argininosuccinate Lyase
Category: 組換えモノクローナル抗体 Tags: , , , , , , ,
Argininosuccinate Lyase Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IP
Reaktivite
Human,Mouse,Rat
Gen Adı
Argininosuccinate Lyase
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Argininosuccinate Lyase 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 Argininosuccinate Lyase
Alternatif İsimler ASAL; Arginosuccinase; ASL
Gen Kimliği 435, 109900, 59085
SwissProt Kimliği P04424, Q91YI0, P20673
İmmünojen A synthetic peptide of human Argininosuccinate Lyase
Uygulama
Uygulama WB,IP
Seyreltme Oranı WB 1:500-1:2000,IP 1:20-1:50
Moleküler Ağırlık Calculated MW:52 kDa; Observed MW:52 kDa
Araştırma Alanı
Arka Plan
This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
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