FA2H antibody (AA 101-150)

Catalog No. ABIN7228460

The Rabbit Polyclonal anti-FA2H antibody has been validated for WB and ELISA. It is suitable to detect FA2H in samples from Human, Mouse and Rat.

Quick Overview for FA2H antibody (AA 101-150) (ABIN7228460)

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 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of FA2H

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

Immunogen: Synthesized peptide derived from part region of human FA2H protein at AA range: 101-150

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 (1:10000-1:20000).

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 as stabilizer.

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 FA2H

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

Alternative Name: FA2H

Background: Rabbit Anti-FA2H Polyclonal Antibody,Fatty acid 2-hydroxylase, Fatty acid alpha-hydroxylase,FA2H 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 FA2H have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.,FA2H

Molecular Weight: observerd band 55kDa

Gene ID: 79152

UniProt: Q7L5A8