ACSL5 antibody (AA 460-540)

Catalog No. ABIN7227196

This Rabbit Polyclonal antibody specifically detects ACSL5 in ELISA and WB. It exhibits reactivity toward Human, Rat and Mouse.

Quick Overview for ACSL5 antibody (AA 460-540) (ABIN7227196)

Target: ACSL5 (Acyl-CoA Synthetase Long-Chain Family Member 5 (ACSL5))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ACSL5 antibody is un-conjugated

Application: ELISA, Western Blotting (WB)

Product Details anti-ACSL5 Antibody

Binding Specificity: AA 460-540

Purpose: Rabbit Anti-ACSL5 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of ACSL5 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 ACSL5 protein at AA range: 460-540

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 ACSL5

Target: ACSL5 (Acyl-CoA Synthetase Long-Chain Family Member 5 (ACSL5))

Alternative Name: ACSL5

Background: Long-chain-fatty-acid--CoA ligase 5, Long-chain acyl-CoA synthetase 5, LACS 5ACSL5 (Acyl-CoA Synthetase Long Chain Family Member 5) is a Protein Coding gene. Diseases associated with ACSL5 include Glioma and Chronic Intestinal Vascular Insufficiency. Among its related pathways are Metabolism and Fatty acid metabolism. The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme is highly expressed in uterus and spleen, and in trace amounts in normal brain, but has markedly increased levels in malignant gliomas.

Molecular Weight: 75kD

Gene ID: 51703

UniProt: Q9ULC5