CCDC11 anticorps (AA 330-380) (AbBy Fluor® 555)

N° du produit ABIN2172321

Cet anticorps anti-CCDC11 est un anticorps Lapin Polyclonal détectant CCDC11 dans WB, IF (cc) et IF (p). Adapté pour Humain et Souris.

Aperçu rapide pour CCDC11 anticorps (AA 330-380) (AbBy Fluor® 555) (ABIN2172321)

Antigène: CCDC11 (Coiled-Coil Domain Containing 11 (CCDC11))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC11 est conjugé à/à la AbBy Fluor® 555

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

Détail du produit anti-CCDC11 anticorps (AbBy Fluor® 555)

Épitope: AA 330-380

Specificité: Due to the similarity of this protein to RWD domain-containing protein 1, there is a chance that this antibody will react with this protein based on a 75 % non-sequential amino acid similarity.

Réactivité croisée: Humain, Souris, Rat

Homologie: Cow,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CCDC11

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 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: 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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur CCDC11

Antigène: CCDC11 (Coiled-Coil Domain Containing 11 (CCDC11))

Autre désignation: Ccdc11

Sujet:

Synonyms: HTX6, CCDC11, Coiled-coil domain-containing protein 11

Background: CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.

ID gène: 220136

UniProt: Q96M91