FA2H antibody (AA 101-150)

Catalog No. ABIN8121400

The Rabbit Polyclonal anti-FA2H antibody (ABIN8121400) specifically detects FA2H in WB and ELISA. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for FA2H antibody (AA 101-150) (ABIN8121400)

Target: FA2H (Fatty Acid 2-Hydroxylase (FA2H))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FA2H antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-FA2H Antibody

Binding Specificity: AA 101-150

Purpose: FA2H Antibody

Specificity: FA2H Polyclonal Antibody detects endogenous levels of FA2H

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

Immunogen: Synthesized peptide derived from human FA2H. at AA range: 101-150

Isotype: IgG

Application Details

Application Notes: WB 1:500-2000, ELISA 1:10000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Liquid in 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: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for FA2H

Target: FA2H (Fatty Acid 2-Hydroxylase (FA2H))

Alternative Name: FA2H

Background:

Synonyms: Fatty acid 2-hydroxylase (EC 1.-.-.-) (Fatty acid alpha-hydroxylase)

Background: This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.[provided by RefSeq, Mar 2010],

Gene Name: FA2H

Protein Name: FA2H

Gene ID: 79152

UniProt: Q7L5A8