HGD Rabbit mAb (AMR11341N)
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.
We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality HGD Rabbit mAb (AMR11341N) .
HGD; AKU; HGO; homogentisate 1; 2-dioxygenase
3081
Q93099
WB 1:500 - 1:2000
Liquid
Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
Calculated MW: 48kDa Observed MW: 50KDa
Store at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=3081
https://www.uniprot.org/uniprot/Q93099
Email for sequence
Beschrijving
HGD Rabbit mAb (AMR11341N) Beschikbaar in 50 µL. Bestel eenvoudig online met snelle levering.
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