GORAB antibody (AA 201-300) (AbBy Fluor® 555)

Catalog No. ABIN914583

Product Details anti-GORAB Antibody (AbBy Fluor® 555)

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

Binding Specificity: AA 201-300

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GORAB antibody is conjugated to AbBy Fluor® 555

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

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SCYL1BP1

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for GORAB

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

Alternative Name: SCYL1BP1 (GORAB Products)

Synonyms: GO antibody, NTKLBP1 antibody, SCYL1BP1 antibody, AI467484 antibody, NTKL-BP1 antibody, Scyl1bp1 antibody, golgin, RAB6 interacting antibody, golgin, RAB6-interacting antibody, GORAB antibody, Gorab antibody

Background:

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.

Gene ID: 92344

UniProt: Q5T7V8