HGD Antibody
Product Specifications
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.
NCBI Gene ID
3081
Swiss Prot
Q93099
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 226-445 of human HGD (NP_000178.2) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Signal Transduction
Purification
Affinity purification
Positive Control
SKOV3
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 50kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
HGD
NCBI Official Name
Homogentisate 1,2-dioxygenase
NCBI Organism
Homo sapiens
Other Product Names
AKU, HGO, homogentisate 1,2-dioxygenase, homogentisate oxidase, homogentisate oxygenase, homogentisic acid oxidase, homogentisicase
Tested Applications
WB
Physical Properties
Liquid
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