Anti-SMARCC1/BAF155 antibody [EPR25109-77]
- BOND RX™ Validated
- 20ul selling size
- RabMAb
- Recombinant
- KO Validated
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(3 Publications)
Knockout Tested Rabbit Recombinant Monoclonal SMARCC1/BAF155 antibody. Suitable for WB, IHC-P, ICC/IF, IP and reacts with Human, Mouse, Rat samples. Cited in 3 publications.
View Alternative Names
BAF155, SMARCC1, SWI/SNF complex subunit SMARCC1, BRG1-associated factor 155, SWI/SNF complex 155 kDa subunit, SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily C member 1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on human colon (PMID : 30144500).The section was incubated with ab305037 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized SMARCC1 KO HeLa (SMARCC1 knockout human cervical adenocarcinoma epithelial cell) (ab264859) cells labelling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing no staining in SMARCC1 knockout Hela cells and showing nuclear staining in wildtype Hela cells.The image was taken with a confocal microscope (Leica-Microsystems, TCS SP8) is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5 ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunohistochemical analysis of paraffin-embedded (A) Wild-type Hela ( tissue labeling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on (A) Wild-type Hela (human cervix adenocarcinoma epithelial cell) cell pellet, and no staining on (B) SMARCC1 knockout Hela (ab264859) cell pellet.The section was incubated with ab305037 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on human kidney (PMID : 33532313).The section was incubated with ab305037 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
SMARCC1/BAF155 was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate 10 ug with ab305037 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab305037 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate 10 ug Lane 2 : ab305037 IP in HeLa whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab305037 in HeLa whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 76 seconds The band beneath the target band (150 kDa) is likely to be degraded target fragments.
All lanes:
Immunoprecipitation - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (ab305037) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate 10 ug
Lane 2:
ab305037 IP in HeLa whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Predicted band size: 150 kDa
Observed band size: 150 kDa
false
Exposure time: 76s
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labeling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on rat spleen.The section was incubated with ab305037 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized ES-D3 [D3] (mouse blastocyst-derived embryonic stem cell) cells labelling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing nuclear staining in ES-D3 [D3] cell line.The image was taken with a confocal microscope (Leica-Microsystems, TCS SP8) is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5 ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunohistochemical analysis of paraffin-embedded Rat colon tissue labeling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on rat colon.The section was incubated with ab305037 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunohistochemical analysis of paraffin-embedded Mouse colon tissue labeling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on mouse colon.The section was incubated with ab305037 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling SMARCC1/BAF155 with ab305037 at 1/100 (4.75 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on mouse spleen.The section was incubated with ab305037 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
SMARCC1/BAF155 was immunoprecipitated from 0.35 mg ES-D3 (mouse embryonic pluripotent stem Cell), whole cell lysate 10 ug with ab305037 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab305037 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : ES-D3 (mouse embryonic pluripotent stem Cell), whole cell lysate 10 ug Lane 2 : ab305037 IP in ES-D3 whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab305037 in ES-D3 whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 15 seconds The band beneath the target band (150 kDa) is likely to be degraded target fragments.
All lanes:
Immunoprecipitation - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (ab305037) at 1/1000 dilution
Lane 1:
ES-D3 (mouse embryonic pluripotent stem Cell), whole cell lysate 10 ug
Lane 2:
ab305037 IP in ES-D3 whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Predicted band size: 150 kDa
Observed band size: 150 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Blocking and diluting buffer and concentration : 5% NFDM/TBST In Western blot, ab305037 was shown to bind specifically to SMARCC1/BAF155. A band was observed at 150 kDa in wild-type HeLa cell lysate whereas no signal observed at this size in SMARCC1/BAF155 knockout cell line. The band beneath the target band (150 kDa) is likely to be degraded target fragments. ES-D3 cell Lysate was freshly made and used immediately to minimize protein degradation. Exposure time : Lanes 1-2 : 26 seconds Lane 3 : 6 seconds
All lanes:
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (ab305037) at 1/1000 dilution
Lane 1:
Wild-type HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 2:
SWI/SNF complex subunit SMARCC1 knockout HeLa, whole cell lysate at 20 µg
Lane 3:
ES-D3 (mouse embryonic pluripotent stem Cell), whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 123 kDa
Observed band size: 150 kDa
false
- WB
Supplier Data
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Blocking and diluting buffer and concentration : 5% NFDM/TBST Lysates were freshly made and used immediately to minimize protein degradation. Samples are non-boiled as boiling may cause protein aggregation. The band beneath the target band (150 kDa) is likely to be degraded target fragments. Exposure time : 26 seconds
All lanes:
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (ab305037) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 2:
293T (human embryonic kidney epithelial cell), whole cell lysate at 20 µg
Lane 3:
NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 20 µg
Lane 4:
PC-12 (rat adrenal gland pheochromocytoma), whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 123 kDa
Observed band size: 150 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Blocking and diluting buffer and concentration : 5% NFDM/TBST Lysates were freshly made and used immediately to minimize protein degradation. The band beneath the target band (150 kDa) is likely to be degraded target fragments. Exposure time : 26 seconds
All lanes:
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (ab305037) at 1/1000 dilution
All lanes:
Mouse spleen tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 123 kDa
Observed band size: 150 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (AB305037)
Blocking and diluting buffer and concentration : 5% NFDM/TBST This antibody does not cross-react with mouse SMARCC2/BAF170. Exposure time : 37 seconds
All lanes:
Western blot - Anti-SMARCC1/BAF155 antibody [EPR25109-77] (ab305037) at 1/1000 dilution
Lane 1:
His-tagged mouse SMARCC1/BAF155 recombinant protein at 10 ng
Lane 2:
His-tagged mouse SMARCC2/BAF170 recombinant protein at 15 ng
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 123 kDa
Observed band size: 50 kDa
false
Exposure time: 37s
Related conjugates and formulations (1)
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Anti-SMARCC1/BAF155 antibody [EPR25109-77] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
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Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SMARCC1 participates in remodeling chromatin architecture to facilitate or repress gene transcription. It forms an integral part of the SWI/SNF complex which is critical for maintaining proper chromatin structure and function. This complex influences gene expression during developmental processes cell cycle regulation and DNA repair. SMARCC1 interacts with other core components of the SWI/SNF complex such as BAF47 and BRG1 ensuring correct and responsive chromatin modification.
Pathways
SMARCC1 participates in the ATP-dependent chromatin remodeling pathway an important player in gene expression control. This remodeling is connected to the cell cycle pathway as it regulates genes required for cell proliferation. Within these pathways SMARCC1 closely interacts with transcription factors such as c-Myc and other chromatin regulators coordinating the expression of target genes necessary for cell growth and differentiation.
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Target data
Publications (3)
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Nature communications 15:6200 PubMed39043686
2024
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Physiological reports 12:e16057 PubMed38825580
2024
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Clinical and translational medicine 13:e1235 PubMed37186134
2023
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