WTX anticorps (AA 281-380)

N° du produit ABIN762806

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

Aperçu rapide pour WTX anticorps (AA 281-380) (ABIN762806)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WTX est non-conjugé

Application: ELISA, Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-WTX anticorps

Épitope: AA 281-380

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
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur WTX

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

Autre désignation: Fam123b

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