ARG45274

anti-FATP3 antibody

anti-FATP3 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Overview

Product Description Polyclonal antibody recognizes FATP3
Tested Reactivity Hu, Ms
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name FATP3
Antigen Species Human
Immunogen Recombinant protein containing to human FATP3.
Conjugation Un-conjugated
Alternate Names SLC27A3; Solute Carrier Family 27 Member 3; ACSVL3; FATP3; Solute Carrier Family 27 (Fatty Acid Transporter), Member 3; Very Long-Chain Acyl-CoA Synthetase Homolog 3; Long-Chain Fatty Acid Transport Protein 3; Long-Chain-Fatty-Acid--CoA Ligase; Arachidonate--CoA Ligase; MGC4365; VLCS-3; Fatty Acid Transport Protein 3; EC 6.2.1.15; EC 6.2.1.3; EC 6.2.1.-; EC 6.2.1.7 47; EC 6.2.1 47; FATP-3

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P2-5 μg/ml
WB0.25-0.5 μg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 70-79 kDa

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer 0.2% Na2HPO4, 0.9% NaCl and 4% Trehalose.
Stabilizer 4% Trehalose
Concentration 0.5 mg/ml
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 or below. 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: 11000 Human SLC27A3

GeneID: 26568 Mouse SLC27A3

Swiss-port # O88561 Mouse Long-chain fatty acid transport protein 3

Swiss-port # Q5K4L6 Human Long-chain fatty acid transport protein 3

Gene Symbol SLC27A3
Gene Full Name Solute Carrier Family 27 Member 3
Background This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]
Function Mainly functions as an acyl-CoA ligase catalyzing the ATP-dependent formation of fatty acyl-CoA using LCFA and very-long-chain fatty acids (VLCFA) as substrates. [UniProt]
Cellular Localization Mitochondrion inner membrane [UniProt]
Calculated MW 74 kDa