ARG40065

anti-FA2H antibody

anti-FA2H antibody for Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes FA2H
Tested Reactivity Hu, Ms
Tested Application WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name FA2H
Antigen Species Human
Immunogen Recombinant fusion protein corresponding to aa. 95-170 of Human FA2H (NP_077282.3).
Conjugation Un-conjugated
Alternate Names SCS7; SPG35; FAH1; Fatty acid 2-hydroxylase; Fatty acid alpha-hydroxylase; EC 1.-.-.-; FAXDC1; FAAH

Application Instructions

Application Suggestion
Tested Application Dilution
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control HT-29
Observed Size 38 kDa

Properties

Form Liquid
Purification Affinity purified.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 338521 Mouse FA2H

GeneID: 79152 Human FA2H

Swiss-port # Q5MPP0 Mouse Fatty acid 2-hydroxylase

Swiss-port # Q7L5A8 Human Fatty acid 2-hydroxylase

Gene Symbol FA2H
Gene Full Name fatty acid 2-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]
Function Required for alpha-hydroxylation of free fatty acids and the formation of alpha-hydroxylated sphingolipids. [UniProt]
Cellular Localization Endoplasmic reticulum membrane; Multi-pass membrane protein. Microsome membrane; Multi-pass membrane protein. [UniProt]
Calculated MW 43 kDa

Images (1) Click the Picture to Zoom In

  • ARG40065 anti-FA2H antibody WB image

    Western blot: 25 µg of HT-29 cell lysate stained with ARG40065 anti-FA2H antibody at 1:1000 dilution.