Learn More
Invitrogen™ HGD Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA593100
Description
Immunogen sequence: DFLIPIAWYE DRQVPGGYTV INKYQGKLFA AKQDVSPFNV VAWHGNYTPY KYNLKNFMVI NSVAFDHADP SIFTVLTAKS VRPGVAIADF VIFPPRWGVA DKTFRPPYYH RNCMSEFMGL IRGHYEAKQG GFLPGGGSLH STMTPHGPDA DCFEKASKVK LAPERIADGT MAFMFESSLS LAVTKWGLKA SRCLDENYHK CWEPLKSHFT PNSRNPAEPN; Positive Samples: SKOV3.
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.
Specifications
HGD | |
Polyclonal | |
Unconjugated | |
HGD | |
aku; alkaptonuria; HGD; HGO; homogentisate 1, 2-dioxygenase; homogentisate 1,2-dioxygenase; homogentisate oxidase; homogentisate oxygenase; Homogentisic acid oxidase; homogentisicase | |
Rabbit | |
Affinity Chromatography | |
RUO | |
3081 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
ELISA, Western Blot | |
0.72 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
Q93099 | |
HGD | |
Recombinant fusion protein containing a sequence corresponding to amino acids 226-445 of human HGD (NP_0001782). | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
Your input is important to us. Please complete this form to provide feedback related to the content on this product.