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The antibody against UROD was raised in rabbit using the Human UROD as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
The antibody against UROD was raised in rabbit using the Human UROD as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB.
$600.00
| Cat.No | ADC-51413A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | UROD |
| Target Synonyms | DCUP_HUMAN antibody; PCT antibody; UPD antibody; URO D antibody; URO-D antibody; urod antibody; Uroporphyrinogen decarboxylase antibody; Uroporphyrinogen III decarboxylase antibody | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium Azide | Purification Method | Antigen affinity purified |
| Conjugate | Non-conjugated | Application | ELISA, WB |
| Storage | Upon receipt |
| Immunogen Description | Human UROD | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | P06132 |
Uniprot Id
P06132
Target Species
Human
Target Name
UROD
Target Full Name
Uroporphyrinogen decarboxylase
Target Function
Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III.
Target Involvement
Familial porphyria cutanea tarda (FPCT); Hepatoerythropoietic porphyria (HEP)
Target Subcellular Location
Cytoplasm.
Target Protein Families
Uroporphyrinogen decarboxylase family
Target Synonyms
DCUP_HUMAN; PCT; UPD; URO D; URO-D; urod; Uroporphyrinogen decarboxylase; Uroporphyrinogen III decarboxylase
Target Background
This gene encodes an enzyme in the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria.
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