Tyrosinase Rabbit pAb - A13608
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Catalog #
AB-A13608
Ab
100,00 €
The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.
| Isotype | IgG |
|---|---|
| Datasheet URL | https://abclonal.com/instructions/pdf/A13608 |
| Alternative Names | ATN; CMM8; OCA1; OCA1A; OCAIA; SHEP3; Tyrosinase |
| Species | Human |
| Source | Rabbit |
| Purity | Affinity purification |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 20-340 of human Tyrosinase (NP_000363.1). |
| Storage | Store at -20℃. Avoid freeze / thaw cycles.|Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |
| Conjugate | Unconjugated |