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The antibody against UROD was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-367 of human UROD (NP_000365.3) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against UROD was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-367 of human UROD (NP_000365.3) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-03763A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | UROD |
| Target Synonyms | PCT; UPD; UROD | Form | Liquid |
| Species Reactivity | Human, Mouse | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Mouse heart, Mouse kidney, HepG2, K-562, Mouse liver, Mouse testis, SW480, SW620 | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 1-367 of human UROD (NP_000365.3). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | P06132 | Immunogen Sequence |
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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