PNKD antibody (AA 140-220)

Catalog No. ABIN7230718

This Rabbit Polyclonal antibody specifically detects PNKD in ELISA and WB. It exhibits reactivity toward Human and Mouse.

Quick Overview for PNKD antibody (AA 140-220) (ABIN7230718)

Target: PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PNKD antibody is un-conjugated

Application: ELISA, Western Blotting (WB)

Product Details anti-PNKD Antibody

Binding Specificity: AA 140-220

Purpose: Rabbit Anti-PNKD Polyclonal Antibody

Specificity: The antibody detects endogenous levels of PNKD protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human PNKD protein at AA range: 140-220

Isotype: IgG

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Preservative: ProClin

Precaution of Use: This product contains ProClin: 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.

Expiry Date: 12 months

Target Details for PNKD

Target: PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))

Alternative Name: PNKD

Background: Probable hydrolase PNKD, Myofibrillogenesis regulator 1, MR-1, Paroxysmal nonkinesiogenic dyskinesia protein, Trans-activated by hepatitis C virus core protein 2PNKD (Paroxysmal Nonkinesigenic Dyskinesia) is a Protein Coding gene. Diseases associated with PNKD include Familial Paroxysmal Nonkinesigenic Dyskinesia and Paroxysmal Nonkinesigenic Dyskinesia 1. PNKD is thought to play a role in the regulation of myofibrillogenesis. Mutations in PNKD have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants.

Molecular Weight: 42kD

Gene ID: 25953

UniProt: Q8N490