CLSTN1 Antibody

• Catalog Number: orb1474454
• Category: Antibodies
• Description: The CLSTN1 Antibody is suitable for IF, IHC, WB. It is a Monoclonal, Unconjugated antibody which raised against A synthetic peptide of human CLSTN1 .Purification: The antibody was purified by immunogen affinity chromatography.
• Clonality: Monoclonal
• Species/Host: Rabbit
• Conjugation: Unconjugated
• Reactivity: Hamster, Human, Mouse
• Form/Appearance: Liquid in 50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 50% Glycerol, 0.01% Sodium azide and 0.05% rAlbumin.
• Purification: The antibody was purified by immunogen affinity chromatography.
• Immunogen: A synthetic peptide of human CLSTN1
• UniProt ID: Q9EPL2, O94985
• Tested applications: IF, IHC, WB
• Dilution range: WB (1/500 - 1/1000), IH (1/50 - 1/100), IF/IC (1/50 - 1/100)
• Antibody Type: Primary Antibody
• Storage: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
• Alternative names: CS1; KIAA0911; Calsyntenin-1; Alcadein-alpha; Alc-
• Note: For research use only
• Entrez: 65945, 22883

Western blot analysis of CLSTN1 expression in mouse brain (A), Hela (B), CHOK1 (C) whole cell lysates. (Predicted band size: 110 kD; Observed band size: 115 kD)

Immunohistochemical analysis of CLSTN1 staining in human colon cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.65). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunofluorescent analysis of CLSTN1 staining in HeLa cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark.