ARID1A, Abcam, ab182560

Abcam ab182560 · ARID1A · mAb · Rabbit
4.03
(Overall rating from 2 reviews)
#2 of 18 targeting ARID1A
4.03
From 2 reviews · #2 of 18 for ARID1A

What do reviewers generally think about ab182560 from Abcam?

Researchers report ab182560 works for detecting endogenous ARID1A by Western blotting in mouse and human cells, with KO-specific loss of signal, and for IP and IF in human HAP1 cells. One reviewer points out that the Western blot signal appears as a cluster of closely migrating bands rather than a single distinct band, and IP does not completely deplete antigen. Overall, it is rated favorably for KO validation and specific detection, with minor notes on band pattern and incomplete depletion.

Information about this antibody

Target
Alt. Targets
N/A
Vendor
Catalog No
ab182560
Clonality
mAb
Origin
Rabbit
Reactivity
Mouse, Human, Rat
Conjugation
N/A
Product Link
N/A
Clone ID
EPR13501

Vendor notes

No vendor notes available for this antibody.

pAbmAbs Average Ratings

ℹ
Western Blot
3.84
Immunostaining
4.08
IP
3.20
Overall
4.03
Add your own rating

User Reviews (2)

Review of: ARID1A, Abcam, ab182560 by pAbmAbs Data Mining

Reviewed: October 19, 2026

Our team has carried out deep research in the published scientific literature to identify papers and reports using antibodies directed against human AT-rich interactive domain-containing protein 1A (ARID1A) and followed up by extraction and evaluation of the available data to assess its performance according to pAbmAbs rating criteria.

YCharOS is here conducting a large head-to-head study comparing 14 commercial research antibodies against human AT-rich interactive domain-containing protein 1A (ARID1A).

The collection of antibodies was tested using HAP1 WT and ARID1A KO cells in the applications WB (WT and KO cell lysates/30 µg protein), IP (WT cell lysate) and IF (WT and KO cells) according to YCharOS standard protocols (see reference).

In WB (1:1000 ab dilution) ab182560 detects a WT-specific signal at the expected high-molecular-weight region (~245 kDa), which is absent in the knockout sample. The immunoreactive signal appears as a cluster of closely migrating bands rather than a single distinct band. A band was detected following IP (2 µg Ab used), this band was more intense compared to band in input extract (6% of starting material). A faint band was also detected in immunodepleted extract (6% of total unbound fraction), showing that the antibody does not completely deplete the antigen from cell lysate. In IF (1:2000 ab dilution), staining was observed in WT cells only.

Western Blot
Immunostaining
IP

Review of: ARID1A, Abcam, ab182560 by Astrid Francisca Jacobsen

Reviewed: September 7, 2026
I am sharing a pAbmAbs generated literature review of KO validated antibodies. Here citing Riou et al. Chromosome and Gene expression, Developmental Biology, 2020. Riou et al. validated this antibody for the detection of endogenous mouse ARID1A by Western blotting using hepatocyte cell lysates from control and ARID1A-KO mice. A clear ARID1A-specific band was detected in control samples, while no corresponding band was observed in ARID1A-KO hepatocytes (Figure 5—figure supplement 2F). Based on the available data, we have assigned a five-star rating but we highly encourage other scientists to share their observations.
Western Blot

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