CLN5 antibody (AA 140-220)

Catalog No. ABIN7219404

This anti-CLN5 antibody is a Rabbit Polyclonal antibody detecting CLN5 in WB and ELISA. Suitable for Human, Mouse and Rat.

Quick Overview for CLN5 antibody (AA 140-220) (ABIN7219404)

Target: CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CLN5 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CLN5 Antibody

Binding Specificity: AA 140-220

Purpose: CLN5 Polyclonal Antibody

Specificity: CLN5 Polyclonal Antibody detects endogenous levels of CLN5 protein.

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

Immunogen: Synthesized peptide derived from the Internal region of human CLN5 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 (1:10000). Not yet tested in other applications.

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.

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 CLN5

Target: CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))

Alternative Name: CLN5

Background: Rabbit Anti-CLN5 Polyclonal Antibody,CLN5, Ceroid-lipofuscinosis neuronal protein 5, Protein CLN5,CLN5 is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.,Ceroid-lipofuscinosis neuronal protein 5

Molecular Weight: observerd band 48kDa

Gene ID: 1203

UniProt: O75503