FZD9 antibody (AA 27-591) (Fluoro647)

Catalog No. ABIN7991888

The Fluoro647-conjugated Rabbit Polyclonal anti-FZD9 antibody (ABIN7991888) specifically detects FZD9 in FACS. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for FZD9 antibody (AA 27-591) (Fluoro647) (ABIN7991888)

Target: FZD9 (Frizzled Family Receptor 9 (FZD9))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FZD9 antibody is conjugated to Fluoro647

Application: Flow Cytometry (FACS)

Product Details anti-FZD9 Antibody (Fluoro647)

Binding Specificity: AA 27-591

Purpose: Anti-Frizzled 9/FZD9 Antibody Fluoro647 Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins

Predicted Reactivity: Human Frizzled 9,FZD9 shares 95.9%,96.1% amino acid (aa) sequence identity with mouse,rat Frizzled 9,FZD9,respectively.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human Frizzled 9/FZD9 recombinant protein (Position: R27-L591). Human Frizzled 9/FZD9 shares 95.9% and 96.1% amino acid (aa) sequence identity with mouse and rat Frizzled 9/FZD9, respectively.

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for FZD9

Target: FZD9 (Frizzled Family Receptor 9 (FZD9))

Alternative Name: FZD9

Background:

Background: Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.

Gene Full Name: frizzled class receptor 9

Gene ID: 8326

UniProt: O00144

Pathways: WNT Signaling