Phenylalanine Hydroxylase (PAH) Antibody
292.5€ (80 µl)
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935106861
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name
Phenylalanine Hydroxylase (PAH) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx032343
tested applications
ELISA, WB
Description
PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Phenylalanine Hydroxylase (PAH) |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Recommended Dilution | WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified through a protein A column, followed by peptide affinity purification. |
| Size 1 | 80 µl |
| Size 2 | 400 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB |
| Buffer | PBS containing 0.09% sodium azide. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P00439 |
| Background | Antibody anti-PAH |
| Status | RUO |
Descripción
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Phenylalanine Hydroxylase (PAH) Antibody
PAH Antibody is a Rabbit Polyclonal antibody against PAH. PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.
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Phenylalanine Hydroxylase (PAH) Antibody
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