OCA2 Melanosomal Transmembrane Protein (OCA2) Antibody

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Description
OCA2 Antibody is a Rabbit Polyclonal antibody against OCA2. This gene encodes the human homologue of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine - a precursor of melanin. Mutations in this gene result in type 2 oculocutaneous albinism.
Documents del producto
Product specifications
Category | Primary Antibodies |
Immunogen Target | OCA2 Melanosomal Transmembrane Protein (OCA2) |
Host | Rabbit |
Reactivity | Human, Mouse |
Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 20 µl |
Size 2 | 100 µl |
Size 3 | 2 × 100 µl |
Form | Liquid |
Tested Applications | ELISA, WB |
Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | Q04671 |
Gene ID | 4948 |
NCBI Accession | NP_000266.2 |
Background | Antibody anti-OCA2 |
Status | RUO |
Note | Concentration: > 0.2 mg/ml - |
Descripción
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OCA2 Melanosomal Transmembrane Protein (OCA2) Antibody
OCA2 Antibody is a Rabbit Polyclonal antibody against OCA2. This gene encodes the human homologue of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine - a precursor of melanin. Mutations in this gene result in type 2 oculocutaneous albinism.
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OCA2 Melanosomal Transmembrane Protein (OCA2) Antibody
This gene encodes the human homologue of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine a precursor of melanin. Mutations in this gene result in type 2 oculocutaneous albinism. [provided by RefSeq].
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