TCTN2 anticorps (AA 61-160) (AbBy Fluor® 647)

N° du produit ABIN1698599

Détail du produit anti-TCTN2 anticorps (AbBy Fluor® 647)

Antigène: TCTN2 (Tectonic Family Member 2 (TCTN2))

Épitope: AA 61-160

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TCTN2 est conjugé à/à la AbBy Fluor® 647

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Souris

Homologie: Human,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human TCTN2

Isotype: IgG

Information d'application

Indications d'application: 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: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur TCTN2

Antigène: TCTN2 (Tectonic Family Member 2 (TCTN2))

Autre désignation: TCTN2 (TCTN2 Produits)

Synonymes: anticorps fb44f11, anticorps wu:fb44f11, anticorps tect2, anticorps C12orf38, anticorps MKS8, anticorps TECT2, anticorps 4432405B04Rik, anticorps Tect2, anticorps tectonic family member 2, anticorps TCTN2, anticorps tctn2, anticorps Tctn2

Sujet:

Synonyms: C12orf38, FLJ12975, MKS8, OTTHUMP00000239215, OTTHUMP00000239216, Tctn2, TECT2, TECT2_HUMAN, Tectonic family member 2, Tectonic-2.

Background: Defects in TCTN2 are the cause of Meckel syndrome type 8 (MKS8) [MIM:613885]. A disorder characterized by a combination of renal cysts and variably associated features including developmental anomalies of the central nervous system (typically encephalocele), hepatic ductal dysplasia and cysts, and polydactyly.

Pathways: Proton Transport