CD42a antibody (Middle Region)

Catalog No. ABIN7994678

The Rabbit Polyclonal anti-CD42a antibody (ABIN7994678) specifically detects CD42a in WB and IHC. The antibody is reactive with Human and Mouse samples.

Quick Overview for CD42a antibody (Middle Region) (ABIN7994678)

Target: CD42a (GP9) (Glycoprotein IX (Platelet) (GP9))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CD42a antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Grade: Carrier-free

Product Details anti-CD42a Antibody

Binding Specificity: Middle Region

Purpose: Anti-CD42a/GP9 Antibody

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

Predicted Reactivity: Human CD42a,GP9 shares 89.5% amino acid (aa) sequence identity with mouse CD42a,GP9.

Characteristics: Anti-CD42a/GP9 Antibody. Tested in IHC, WB applications. This antibody reacts with Human, Mouse.

Purification: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence in the middle region of human CD42a/GP9. Human CD42a/GP9 shares 89.5% amino acid (aa) sequence identity with mouse CD42a/GP9.

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human, Mouse Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for CD42a

Target: CD42a (GP9) (Glycoprotein IX (Platelet) (GP9))

Alternative Name: GP9

Background:

Background: This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency.

Gene Full Name: glycoprotein IX platelet

Molecular Weight: 19 kDa

Gene ID: 2815

UniProt: P14770