Phenylalanine Hydroxylase Antibody (C4) - BSA Free

Immunohistochemistry-Paraffin: Phenylalanine Hydroxylase Antibody (C4) [NBP3-41889] - DAB staining on IHC-P; Sample: Human Liver Tissue; Primary Ab: 30ug/ml NBP3-41889; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody

Western Blot: Phenylalanine Hydroxylase Antibody (C4) [NBP3-41889] - Sample: Lane1: Human Serum; Lane2: Rat Liver lysate; Lane3: Mouse Gallbladder lysate; Lane4: Hela cell lysate Primary Ab: 2ug/ml NBP3-41889; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody

• Reactivity: Hu, Mu, Rt, Po
• Applications: WB, IHC
• Clone: C4
• Clonality: Monoclonal
• Host: Mouse
• Conjugate: Unconjugated
• Format: BSA Free
• Concentration: 1 mg/ml

Phenylalanine Hydroxylase Antibody (C4) - BSA Free Summary

• Description: Novus Biologicals Mouse Phenylalanine Hydroxylase Antibody (C4) - BSA Free (NBP3-41889) is a monoclonal antibody validated for use in IHC and WB. All Novus Biologicals antibodies are covered by our 100% guarantee.
• Immunogen: Immunized with recombinant Human Phenylalanine Hydroxylase (Uniprot#: P00439; Glu228-Lys452 (Uniprot#: P00439)
• Isotype: IgG1 Kappa
• Clonality: Monoclonal
• Host: Mouse
• Gene: PAH
• Purity: Affinity purified

Applications/Dilutions

• Dilutions:
  • Immunohistochemistry 5-30ug/mL
  • Immunohistochemistry-Paraffin 5-30ug/mL
  • Western Blot 0.01-2ug/mL

Packaging, Storage & Formulations

• Storage: Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
• Buffer: 0.01M PBS, pH7.4, 50% glycerol
• Preservative: 0.05% Proclin 300
• Concentration: 1 mg/ml
• Purity: Affinity purified

Alternate Names for Phenylalanine Hydroxylase Antibody (C4) - BSA Free

• EC 1.14.16
• EC 1.14.16.1
• PH
• phe-4-monooxygenase
• phenylalanine 4-monooxygenase
• phenylalanine hydroxylase
• phenylalanine-4-hydroxylase
• PKU
• PKU1

Background

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.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: PAH