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HGD rabbit pAb - ES15769HGD rabbit pAb Sizes: 50L, 100L Catalogue Numbers: ES15769 50, ES15769 100 Citations, Manuals and MSDS Available upon request. Background: 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.[provided by RefSeq, May 2010], Source: Rabbit Applications: WB
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HGD rabbit pAb
Sizes: 50μL, 100μL
Catalogue Numbers: ES15769-50, ES15769-100
Citations, Manuals and MSDS Available upon request.
Background: 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.[provided by RefSeq, May 2010],
Source: Rabbit
Applications: WB
Dilution: WB 1: 500-2000
Reactivity: Human; Mouse
Immunogen: Synthesized peptide derived from human HGD AA range: 21-71
Storage and Stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human Gene ID: 3081
Human SWISS Prot NO: Q93099
Subcellular Location: cytosol, extracellular exosome,
Research Use Only
HGD rabbit pAb - ES15769
Item no
:
97334794961
US$ 103.60
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