SLC27A2
Reactivité: Humain
Hôte: Lapin
Polyclonal
FITC
Indications d'application
SLC27A2 antibody can be used for detection of SLC27A2 by ELISA at 1:62500. SLC27A2 antibody can be used for detection of SLC27A2 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Restrictions
For Research Use only
Format
Lyophilized
Reconstitution
Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Concentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Conseil sur la manipulation
As with any antibody avoid repeat freeze-thaw cycles.
Stock
4 °C/-20 °C
Stockage commentaire
For short periods of storage (days) store at 4 °C. For longer periods of storage, store SLC27A2 antibody at -20 °C.
Antigène
SLC27A2
(Solute Carrier Family 27 (Fatty Acid Transporter), Member 2 (SLC27A2))
anticorps vlcs, anticorps fatp2, anticorps vlacs, anticorps acsvl1, anticorps facvl1, anticorps im:7139614, anticorps slc27a2, anticorps wu:fb99g05, anticorps zgc:112376, anticorps ACSVL1, anticorps FACVL1, anticorps HsT17226, anticorps hFACVL1, anticorps FATP2, anticorps VLCS, anticorps Vlac, anticorps Vlacs, anticorps VLACS, anticorps solute carrier family 27 (fatty acid transporter), member 2 L homeolog, anticorps solute carrier family 27 member 2, anticorps solute carrier family 27 (fatty acid transporter), member 2a, anticorps solute carrier family 27 (fatty acid transporter), member 2, anticorps slc27a2.L, anticorps SLC27A2, anticorps slc27a2a, anticorps slc27a2, anticorps Slc27a2
Sujet
SLC27A2 is an isozyme of 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 activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy.The protein encoded by this gene is an isozyme of 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 activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy.