ARID1A Recombinant Rabbit Monoclonal Antibody [JJ09-01]
cat.: ET1701-60
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: IF-Cell, IF-Tissue, IHC-P, WB
Clonality: Monoclonal
Clone number: JJ09-01
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 242 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human ARID1A aa 1,184-1,334 / 2,285.
Positive control: K-562 cell lysate, AGS cell lysate, K-562, human colon tissue, mouse colon tissue, rat colon tissue.
Subcellular location: Nucleus.
Recommended Dilutions:
  IF-Cell
  IF-Tissue
  IHC-P
  WB

1:200-1:500
1:50-1:200
1:100-1:500
1:2,000
Uniprot #: SwissProt: O14497 Human | A2BH40 Mouse
Unigene: 61077 Rat
Alternative names: actin-dependent regulator of chromatin subfamily F member 1 ARI1A_HUMAN ARID domain containing protein 1A ARID domain-containing protein 1A ARID1A AT rich interactive domain 1A (SWI like) AT rich interactive domain 1A AT rich interactive domain containing protein 1A AT-rich interactive domain-containing protein 1A B120 BAF250 BAF250A BM029 brain protein 120 BRG1 associated factor 250 BRG1 associated factor 250a BRG1-associated factor 250 BRG1-associated factor 250a C1ORF4 chromatin remodeling factor p250 chromosome 1 open reading frame 4 ELD hELD hOSA1 matrix-associated MRD14 Osa homolog 1 OSA1 OSA1 nuclear protein P270 SMARCF1 SWI like protein SWI SNF complex protein p270 SWI-like protein SWI/SNF complex protein p270 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily f, member 1 SWI/SNF-related
Images
ET1701-60_1.jpg Fig1: Western blot analysis of ARID1A on different lysates with Rabbit anti-ARID1A antibody (ET1701-60) at 1/2,000 dilution.

Lane 1: K-562 cell lysate (20 µg/Lane)
Lane 2: AGS cell lysate (20 µg/Lane)

Predicted band size: 242 kDa
Observed band size: 150-300 kDa

Exposure time: 3 minutes; ECL: K1801;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1701-60) at 1/2,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
ET1701-60_2.jpg Fig2: Immunocytochemistry analysis of K-562 cells labeling ARID1A with Rabbit anti-ARID1A antibody (ET1701-60) at 1/200 dilution.

Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-ARID1A antibody (ET1701-60) at 1/200 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.
ET1701-60_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-ARID1A antibody (ET1701-60) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-60) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1701-60_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse colon tissue with Rabbit anti-ARID1A antibody (ET1701-60) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-60) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET1701-60_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded rat colon tissue with Rabbit anti-ARID1A antibody (ET1701-60) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1701-60) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.