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: PNKD Polyclonal Antibody

Specificity: The antibody detects endogenous levels of PNKD 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 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 (1:500-1:2000), 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 PNKD

Target: PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))

Alternative Name: PNKD

Background: Rabbit Anti-PNKD Polyclonal Antibody,Probable hydrolase PNKD, Myofibrillogenesis regulator 1, MR-1, Paroxysmal nonkinesiogenic dyskinesia protein, Trans-activated by hepatitis C virus core protein 2,PNKD (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.,PNKD

Molecular Weight: observerd band 42kDa

Gene ID: 25953

UniProt: Q8N490