WTX anticorps (AA 281-380) (Biotin)

N° du produit ABIN762808

Détail du produit anti-WTX anticorps (Biotin)

Antigène: WTX (AMER1) (APC Membrane Recruitment Protein 1 (AMER1))

Épitope: AA 281-380

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WTX est conjugé à/à la Biotin

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

Homologie: Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM123B/AMER1

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur WTX

Antigène: WTX (AMER1) (APC Membrane Recruitment Protein 1 (AMER1))

Autre désignation: FAM123B (AMER1 Produits)

Synonymes: anticorps 2810002O09Rik, anticorps AW492303, anticorps Fam123b, anticorps Wtx, anticorps FAM123B, anticorps OSCS, anticorps WTX, anticorps RGD1560322, anticorps fam123b, anticorps APC membrane recruitment 1, anticorps APC membrane recruitment protein 1, anticorps Amer1, anticorps AMER1, anticorps amer1

Sujet:

Synonyms: AMER1, FAM 123B, Family with sequence similarity 123B, FLJ39827, OSCS, Protein FAM123B, RP11 403E24.2, Wilms tumor gene on the X chromosome protein, Wilms tumor on the X, WTX, AMER1_HUMAN.

Background: The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

ID gène: 139285