Tat (Internal Region) anticorps

N° du produit ABIN7224608

Cet anticorps anti-not_set est un anticorps Lapin Polyclonal détectant not_set dans ELISA et IHC (p). Adapté pour Humain, Souris et Rat.

Aperçu rapide pour Tat (Internal Region) anticorps (ABIN7224608)

Antigène: Tat

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Inconjugué

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit

Épitope: Internal Region

Fonction: TAT Polyclonal Antibody

Specificité: TAT Polyclonal Antibody detects endogenous levels of TAT protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen

Immunogène: Synthesized peptide derived from the Internal region of human TAT

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détail du antigène

Antigène: Tat

Classe de substances: Viral Protein

Sujet: Rabbit Anti-TAT Polyclonal Antibody,TAT, Tyrosine aminotransferase, TAT, L-tyrosine:2-oxoglutarate aminotransferase,This nuclear gene TAT (tyrosine aminotransferase) encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in TAT cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked.,Tyrosine aminotransferase

ID gène: 6898

UniProt: P17735