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Anti-JUB / Ajuba Antibody (aa224-239) LS-C19041

Catalog Size Price
LS-C19041-100 100 µg (1.67 mg/ml) Unavailable

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4 JUB / Ajuba Antibodies

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100% Guaranteed
Rabbit Polyclonal to Human JUB / Ajuba
Western blot, ELISA


Human JUB / Ajuba
Human (tested or 100% immunogen sequence identity)
Immunoaffinity purified


  • Western blot (1:500 - 1:2500)
  • ELISA (1:20000 - 1:80000)

Specificity and Use

JUB / Ajuba antibody was raised against synthetic peptide from human JUB / Ajuba.
aa 224-239 of Human Ajuba.
This affinity purified antibody has been tested for use in ELISA and by western blot. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately 57 kD in size corresponding to Ajuba 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.
Store vial at -20 C prior to opening. Dilute only prior to immediate use. For extended storage aliquot contents and freeze at -20 C or below. Avoid cycles of freezing and thawing.
For research use only.

About JUB / Ajuba

Q96IF1 NM_032876 NP_116265.1

AJUBA Antibody, Ajuba LIM protein Antibody, Jub, ajuba homolog Antibody, JUB Antibody, Protein ajuba Antibody

Adapter or scaffold protein which participates in the assembly of numerous protein complexes and is involved in several cellular processes such as cell fate determination, cytoskeletal organization, repression of gene transcription, mitosis, cell-cell adhesion, cell differentiation, proliferation and migration. Contributes to the linking and/or strengthening of epithelia cell-cell junctions in part by linking adhesive receptors to the actin cytoskeleton.

Western blot

Western blot
Anti-Ajuba Antibody - Western Blot. Western blot of Affinity Purified anti-Ajuba antibody shows detection of a 57-kD band consistent with the expected MW for Ajuba (arrowhead). Lanes correspond to 1) HeLa nuclear extract, and 2) HeLa, 3) A431, 4) Jurkat and 5) 293 whole cell lysates. Immunoprecipitation of Ajuba followed by western blotting may result in cleaner background staining. Approximately 5 ug of each preparation was run on a SDS-PAGE and transferred onto nitrocellulose followed by reaction with a 1:500 dilution of anti-Ajuba antibody. Detection occurred using a 1:5000 dilution of HRP-labeled Donkey anti-Rabbit IgG for 1 hour at room temperature. A chemiluminescence system was used for signal detection (Roche) using a 60-sec exposure time. Personal Communication. E. Pugacheva, Fox Chase Cancer Center, Philadelphia, PA.

Western blot

Western blot
Anti-Ajuba Antibody - Western Blot. Western blot of Affinity Purified anti-Ajuba antibody shows detection of Ajuba-RFP fusion protein in cell lysates (arrow-head). Lanes correspond to 1) vector only transfection, 2) human Ajuba-RFP, 3) mouse Ajuba-RFP, and 4) mock transfection. Approximately 50 ug of each lysate was loaded per lane for SDS-PAGE followed by transfer onto nitrocellulose and reaction with a 1:1700 dilution of anti-Ajuba antibody. Detection occurred using a 1:10000 dilution of IRDye800 conjugated Gt-a-Rabbit IgG [H&L] ( for 45 min at room temperature (800 nm channel, green). Molecular weight estimation was made by comparison to prestained MW markers (indicated at left, 700 nm channel, red). IRDye800 fluorescence image was captured using the Odyssey Infrared Imaging System developed by LI-COR. IRDye is a trademark of LI-COR, Inc. Other detection systems will yield similar results.

Requested From: 
Date Requested: 3/21/2018

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