ALDH7A1 Rabbit Monoclonal Antibody

ALDH7A1 Rabbit Monoclonal Antibody

Cat: AMRe87727
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC/IF,FC,IP
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:ALDH7A1
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , , ,
ALDH7A1 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF,FC,IP
Reaktivite
Human,Mouse,Rat
Gen Adı
ALDH7A1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı ALDH7A1 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 ALDH7A1
Alternatif İsimler EPD; PDE; ATQ1
Gen Kimliği 501, 110695
SwissProt Kimliği P49419, Q9DBF1
İmmünojen A synthetic peptide of human ALDH7A1
Uygulama
Uygulama WB,IHC,ICC/IF,FC,IP
Seyreltme Oranı WB 1:2000-1:20000,IHC 1:200-1:2000,ICC/IF 1:20-1:50,FC 1:20-1:50,IP 1:20-1:50
Moleküler Ağırlık Calculated MW:59 kDa; Observed MW:59 kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified. [provided by RefSeq, Jan 2011]
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