HSPB3 antibody (AA 30-110)

Catalog No. ABIN7228978

The Rabbit Polyclonal anti-HSPB3 antibody is suitable to detect HSPB3 in samples from Human, Rat and Mouse. It has been validated for WB and ELISA.

Quick Overview for HSPB3 antibody (AA 30-110) (ABIN7228978)

Target: HSPB3 (Heat Shock 27kDa Protein 3 (HSPB3))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HSPB3 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-HSPB3 Antibody

Binding Specificity: AA 30-110

Purpose: Rabbit Anti-HSPB3 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of HSPB3 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 HSPB3 protein at AA range: 30-110

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 HSPB3

Target: HSPB3 (Heat Shock 27kDa Protein 3 (HSPB3))

Alternative Name: HSPB3

Background: Heat shock protein beta-3, HspB3, Heat shock 17 kDa protein, HSP 17, Protein 3HSPB3 encodes a muscle-specific small heat shock protein. A mutation in this gene is the cause of autosomal dominant distal hereditary motor neuropathy type 2C. HSPB3 (Heat Shock Protein Family B (Small) Member 3) is a Protein Coding gene. Diseases associated with HSPB3 include Neuronopathy, Distal Hereditary Motor, Type Iic and Distal Hereditary Motor Neuropathy, Type Ii. An important paralog of this gene is HSPB2-C11orf52.

Molecular Weight: 16kD

Gene ID: 8988

UniProt: Q12988