UBIAD1 anticorps (AA 210-260)

N° du produit ABIN5690308

L’anticorps Lapin Polyclonal anti-UBIAD1 a été validé pour WB, ELISA, IF et IHC (p). Il convient pour détecter UBIAD1 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour UBIAD1 anticorps (AA 210-260) (ABIN5690308)

Antigène: UBIAD1 (UbiA Prenyltransferase Domain Containing 1 (UBIAD1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp UBIAD1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-UBIAD1 anticorps

Épitope: AA 210-260

Specificité: UBIAD1 antibody is human, mouse and rat reactive.

Purification: UBIAD1 antibody is affinity chromatography purified via peptide column.

Immunogène: UBIAD1 antibody was raised against a 15 amino acid peptide near the carboxy terminus of human UBIAD1.

The immunogen is located within amino acids 210 - 260 of UBIAD1.

Isotype: IgG

Information d'application

Indications d'application: UBIAD1 antibody can be used for detection of UBIAD1 by Western blot at 1 - 2 μ,g/mL. Antibody can also be used for Immunohistochemistry at 5 μ,g/mL. For Immunoflorescence start at 20 μ,g/mL.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: UBIAD1 Antibody is supplied in PBS containing 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: 4 °C,-20 °C

Stockage commentaire: UBIAD1 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.

Détails sur UBIAD1

Antigène: UBIAD1 (UbiA Prenyltransferase Domain Containing 1 (UBIAD1))

Autre désignation: UBIAD1

Sujet: The UbiA prenyltransferase domain containing 1 (UBIAD1) protein , also known as TERE1, was initially identified as a down-regulated gene in transitional cell carcinoma of the bladder (1). Recently it has been shown to bind the cholesterol carrier APOE and modulate cellular cholesterol levels (2). Mutations in the UBIAD1 gene can cause Schnyder crystalline corneal dystrophy, an autosomal dominant disease characterized by progressive opacification of the cornea resulting from the local accumulation of lipids (3).

Poids moléculaire: Predicted: 37 kDa

Observed: 45 kDa

ID gène: 29914

NCBI Accession: NP_037451

UniProt: Q9Y5Z9