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Anti-ASAP3 Antibody LS-C59552


Wt. Vol. Conc. Price
100 µg - - Unavailable

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Rabbit Polyclonal to Human ASAP3
Western blot, ELISA


Human ASAP3
Human (tested or 100% immunogen sequence identity)
Protein A purified


  • Western blot (1:1000 - 1:10000)
  • ELISA (1:1000 - 1:5000)

Specificity and Use

ASAP3 antibody was raised against recombinant human UPLC1/ASAP3 protein.
human UPLC1/ASAP3 protein. A BLAST analysis was used to suggest cross-reactivity with UPLC1/ASAP3 protein from mouse and rat based on approximately 80% homology with the human protein. Reactivity against homologs from other sources is not known
This protein A purified antibody has been tested for use in ELISA and western blotting. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately 100 kD in size corresponding to UPLC1/ASAP3 protein by western blotting in the appropriate cell lysate or extract.


0.02 M potassium phosphate, 0.15 M sodium chloride, pH 7.2, 0.01% sodium azide.
Long term: -20°C; Short term: -20°C
For research use only.

About ASAP3

Q8TDY4 NM_017707 NP_060177.2

ASAP3 Antibody, ACAP4 Antibody, ARF6 GTPase-activating protein Antibody, CENTB6 Antibody, DDEFL1 Antibody, Centaurin, beta 6 Antibody, UPLC1 Antibody

ASAP3 is a member of a subfamily of ADP-ribosylation factor(Arf) GTPase-activating proteins that contain additional ankyrin repeat and pleckstrin homology domains. The Arf GAP domain of this protein catalyzes the hydrolysis of GTP bound to Arf proteins. The encoded protein promotes cell differentiation and migration and has been implicated in cancer cell invasion. Alternative splicing results in multiple transcript variants.

Western blot

Western blot
Anti-UPLC1/ASAP3 Antibody - Western Blot. Western blot of protein A purified anti-UPLC1/ASAP3 antibody shows detection of UPLC1/ASAP3 in NIH/3T3 cells over-expressing the protein. Cell extracts (5 ug) were resolved by electrophoresis and transferred to nitrocellulose. The membrane was probed with anti-UPLC1/ASAP3 at a 1:10000 dilution. Personal Communication, Vi Luan HA, CCR-NCI, Bethesda, MD.

Requested From: 
Date Requested: 4/25/2017

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