Phenylalanine Hydroxylase (PAH) Antibody
195€ (20 µl)
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935106861
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name
Phenylalanine Hydroxylase (PAH) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx001310
tested applications
ELISA, WB, IF/ICC
Description
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.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Phenylalanine Hydroxylase (PAH) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/1000, IF/ICC: 1/50 - 1/200. 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, IF/ICC |
| 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 | P00439 |
| Gene ID | 5053 |
| NCBI Accession | NP_000268.1 |
| Background | Antibody anti-PAH |
| Status | RUO |
| Note | Concentration: > 0.2 mg/ml - |
Descripción
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Human PAH(Phenylalanine Hydroxylase) ELISA Kit
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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.
Ver Producto
Phenylalanine Hydroxylase (PAH) Antibody
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.
Ver Producto