PHF21B antibody (AA 291-499)

Catalog No. ABIN8021007

The Rabbit Polyclonal anti-PHF21B antibody is suitable to detect PHF21B in samples from Human. It has been validated for WB, IF, ELISA and ICC.

Quick Overview for PHF21B antibody (AA 291-499) (ABIN8021007)

Target: PHF21B (PHD Finger Protein 21B (PHF21B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PHF21B antibody is un-conjugated

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

Grade: Carrier-free

Product Details anti-PHF21B Antibody

Binding Specificity: AA 291-499

Purpose: Anti-PHF21B Antibody

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

Characteristics: Anti-PHF21B Antibody. Tested in ELISA, IF, ICC, WB applications. This antibody reacts with Human.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human PHF21B recombinant protein (Position: E291-M499).

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 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 and 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: Store 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 freeze-thaw cycles.

Expiry Date: 12 months

Target Details for PHF21B

Target: PHF21B (PHD Finger Protein 21B (PHF21B))

Alternative Name: PHF21B

Background:

Background: PHF21B (PHD finger protein 21B), also known as PHF4, is a 531 amino acid protein that contains one PHD-type zinc finger and is expressed as multiple alternatively spliced isoforms. The gene encoding PHF21B maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia.

Gene Full Name: PHD finger protein 21B

Molecular Weight: 57 kDa

Gene ID: 112885

UniProt: Q96EK2