CRTAP antibody

Catalog No. ABIN2856731

The Rabbit Polyclonal anti-CRTAP antibody has been validated for WB, ICC and IF. It is suitable to detect CRTAP in samples from Human.

Quick Overview for CRTAP antibody (ABIN2856731)

Target: CRTAP (Cartilage Associated Protein (CRTAP))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CRTAP antibody is un-conjugated

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Product Details anti-CRTAP Antibody

Cross-Reactivity: Human

Characteristics: Rabbit polyclonal antibody to Cartilage-associated protein (cartilage associated protein)
Cartilage-associated protein antibody [N2C3-2]

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human CRTAP. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: A431

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.79 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for CRTAP

Target: CRTAP (Cartilage Associated Protein (CRTAP))

Alternative Name: cartilage associated protein

Background: The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli. Defects in this gene are associated with osteogenesis imperfecta, a connective tissue disorder characterized by bone fragility and low bone mass.

Cellular Localization: Secreted , extracellular space , extracellular matrix

Molecular Weight: 47 kDa

Gene ID: 10491

UniProt: O75718