Anti-FGD5 Antibody Picoband®
A09444-1
100 μg/vial
Lyophilized
Boster Bio Anti-FGD5 Antibody Picoband® catalog # A09444-1. Tested in WB, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months.Avoid repeated freezing and thawing.
Anti-FGD5 Antibody Picoband® (Boster Biological Technology, Pleasanton CA, USA, Catalog # A09444-1)
Rabbit
Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
Polyclonal
E.coli-derived human FGD5 recombinant protein (Position: Q705-L1462). Human FGD5 shares 86.8% amino acid (aa) sequence identity with mouse FGD5.
A09444-1 is reactive to FGD5 in Human, Mouse, Rat
Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
65 kDa
159.9 kDa
Predicted to enable guanyl-nucleotide exchange factor activity and small GTPase binding activity. Predicted to be involved in actin cytoskeleton organization; filopodium assembly; and regulation of cell shape. Located in plasma membrane.
Boster validates all antibodies on WB, IHC, ICC, Immunofluorescence, and ELISA with known positive control and negative samples to ensure specificity and high affinity, including thorough antibody incubations.
A09444-1 is guaranteed for ELISA, Flow Cytometry, WB Boster Guarantee
The recommendations below provide a starting point for assay optimization. The actual working concentration varies and should be decided by the user.
Western blot, 0.25-0.5 μg/ml, Human, Mouse, Rat
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/ml

Western blot analysis of FGD5 using anti-FGD5 antibody (A09444-1).
Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human 293T whole cell lysates,
Lane 2: human U2OS whole cell lysates,
Lane 3: rat lung tissue lysates,
Lane 4: rat ovary tissue lysates,
Lane 5: mouse lung tissue lysates,
Lane 6: mouse ovary tissue lysates.
After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGD5 antigen affinity purified polyclonal antibody (A09444-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FGD5 at approximately 65 kDa. The expected band size for FGD5 is at 160 kDa.

Flow Cytometry analysis of 293T cells using anti-FGD5 antibody (A09444-1).
Overlay histogram showing 293T cells stained with A09444-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FGD5 Antibody (A09444-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.