CRB1 anticorps (AA 301-400) (AbBy Fluor® 680)

N° du produit ABIN6942646

Détail du produit anti-CRB1 anticorps (AbBy Fluor® 680)

Antigène: CRB1 (Crumbs Homolog 1 (CRB1))

Épitope: AA 301-400

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CRB1 est conjugé à/à la AbBy Fluor® 680

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

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CRB1

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 CRB1

Antigène: CRB1 (Crumbs Homolog 1 (CRB1))

Autre désignation: CRB1 (CRB1 Produits)

Synonymes: anticorps CRB1, anticorps si:dkey-114d20.6, anticorps si:dkey-114d20.7, anticorps LCA8, anticorps RP12, anticorps 7530426H14Rik, anticorps A930008G09Rik, anticorps crumbs 1, cell polarity complex component, anticorps crumbs family member 1, photoreceptor morphogenesis associated, anticorps CRB1, anticorps crb1, anticorps Crb1

Sujet:

Synonyms: CRB1, CRUM1_HUMAN, Protein crumbs homolog 1.

Background: This gene encodes a protein which is similar to the Drosophila crumbs protein and localizes to the inner segment of mammalian photoreceptors. In Drosophila crumbs localizes to the stalk of the fly photoreceptor and may be a component of the molecular scaffold that controls proper development of polarity in the eye. Mutations in this gene are associated with a severe form of retinitis pigmentosa, RP12, and with Leber congenital amaurosis. Alternate splicing results in multiple transcript variants, some protein coding and some non-protein coding.[provided by RefSeq, Apr 2012]

ID gène: 23418

UniProt: P82279

Pathways: Signalisation Notch