Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Preservative: 0.02% Sodium Azide
Constituents: 1% BSA, PBS, pH 7.4
Concentration information loading...
Immunogen affinity purified
Abpromise guarantee covers the use of
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use a concentration of 5 µg/ml.
Use a concentration of 1 µg/ml. Detects a band of approximately 78 kDa (predicted molecular weight: 78 kDa).
Activation of long-chain fatty acids for both synthesis of cellular lipids, and degradation via beta-oxidation. Preferentially uses palmitoleate, oleate and linoleate.
Highly expressed in liver, heart, skeletal muscle, kidney and erythroid cells, and to a lesser extent in brain, lung, placenta and pancreas.
Belongs to the ATP-dependent AMP-binding enzyme family.
Expressed during the early stages of erythroid development while expression is very low in reticulocytes and young erythrocytes.
Mitochondrion outer membrane. Peroxisome membrane. Microsome membrane. Endoplasmic reticulum membrane.
Information by UniProt
ACS 1 antibody
ACSL 1 antibody
Anti-ACSL1 antibody 画像
Western blot - ACSL1 antibody (ab76702)
All lanes :
Anti-ACSL1 antibody (ab76702) at 1 µg/ml
Lane 1 :
Human liver tissue lysate - total protein (
Lane 2 :
Human kidney tissue lysate - total protein (
Lane 3 :
Human heart tissue lysate - total protein (
Lysates/proteins at 10 µg per lane.
Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
Developed using the ECL technique
Performed under reducing conditions.
Predicted band size :
Observed band size :
Additional bands at :
75 kDa (possible isoform).
Exposure time :
Immunocytochemistry/ Immunofluorescence - Anti-ACSL1 antibody (ab76702)
ICC/IF image of ab76702 stained HepG2 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab76702, 5µg/ml) overnight at +4°C. The secondary antibody (green) was
Dylight® 488 goat anti-rabbit IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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