GORAB anticorps (AA 201-300) (AbBy Fluor® 594)

N° du produit ABIN2806237

Détail du produit anti-GORAB anticorps (AbBy Fluor® 594)

Antigène: GORAB (Golgin, RAB6-Interacting (GORAB))

Épitope: AA 201-300

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GORAB est conjugé à/à la AbBy Fluor® 594

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

Réactivité croisée: Humain

Homologie: Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SCYL1BP1

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 GORAB

Antigène: GORAB (Golgin, RAB6-Interacting (GORAB))

Autre désignation: SCYL1BP1 (GORAB Produits)

Synonymes: anticorps GO, anticorps NTKLBP1, anticorps SCYL1BP1, anticorps AI467484, anticorps NTKL-BP1, anticorps Scyl1bp1, anticorps golgin, RAB6 interacting, anticorps golgin, RAB6-interacting, anticorps GORAB, anticorps Gorab

Sujet:

Synonyms: GO, NTKLBP1, SCYL1BP1, RAB6-interacting golgin, N-terminal kinase-like-binding protein 1, NTKL-BP1, NTKL-binding protein 1, hNTKL-BP1, SCY1-like 1-binding protein 1, SCYL1-BP1, SCYL1-binding protein 1, GORAB

Background: Defects in GORAB are the cause of geroderma osteodysplasticum (GO) [MIM:231070], also known as gerodermia osteodysplastica or Walt Disney dwarfism. GO is a rare autosomal recessive disorder characterized by lax, wrinkled skin, joint laxity and a typical face with a prematurely aged appearance. Skeletal signs include severe osteoporosis leading to frequent fractures, malar and mandibular hypoplasia and a variable degree of growth retardation.

ID gène: 92344

UniProt: Q5T7V8