DLL3 antibody (AA 510-590)

Catalog No. ABIN7228240

The Rabbit Polyclonal anti-DLL3 antibody has been validated for WB and ELISA. It is suitable to detect DLL3 in samples from Human, Mouse and Rat.

Quick Overview for DLL3 antibody (AA 510-590) (ABIN7228240)

Target: DLL3 (delta Like Protein 3 (DLL3))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DLL3 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-DLL3 Antibody

Binding Specificity: AA 510-590

Purpose: DLL3 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of DLL3 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human DLL3 protein at AA range: 510-590

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Target Details for DLL3

Target: DLL3 (delta Like Protein 3 (DLL3))

Alternative Name: DLL3

Background: Rabbit Anti-DLL3 Polyclonal Antibody,Delta-like protein 3, Drosophila Delta homolog 3, Delta3,DLL3 encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in DLL3 cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for DLL3.,DLL3

Molecular Weight: observerd band 67kDa

Gene ID: 10683

UniProt: Q9NYJ7

Pathways: Notch Signaling