Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840]
- BOND RX™ Validated
- RabMAb
- Recombinant
- Advanced Validation
- 20ul selling size
- What is this?
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(3 Reviews)
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(49 Publications)
Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327) is a rabbit monoclonal antibody detecting MASH1/Achaete-scute homolog 1 in Western Blot, IP, IHC-P, ICC/IF, ChIP-seq. Suitable for Human, Mouse, Rat.
IHC Leica BOND RXTM protocol - download the protocol
- Biophysical QC for unrivalled batch-batch consistency
- Over 20 publications
View Alternative Names
ASH1, BHLHA46, HASH1, ASCL1, Achaete-scute homolog 1, ASH-1, hASH1, Class A basic helix-loop-helix protein 46, bHLHa46
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of 4% paraformaldehyde-fixed Ascl1CreER/+; ROSA26mTmG/+ mouse thyroid tissue labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 dilution, followed by Tyramide Signal Amplification (red).
Counterstain : DAPI (blue) and chick anti-GFP (green).
ROSA26mTmG/+ mice were bred with Ascl1CreER/+ mice, in which the Ascl1 promoter drives the expression of Cre, to generate mice carrying the genotype of Ascl1CreER/+; ROSA26mTmG/+. Cre activation upon Tamoxifen administration resulted in eGFP expression from the ROSA26mTmG/+ allele. The thyroid tissue from Ascl1CreER/+; ROSA26mTmG/+ mouse was fixed and embedded in paraffin. Paraffin section was stained with rabbit anti-MASH1/Achaete-scute homolog 1 (ab211327) antibody (Red color) and chick anti-GFP antibody (Green color). Tyramide signal amplification was used for high-resolution imaging of low-abundance targets.
The image was kindly provided by our collaborator Dr. Hai Song, Zhejiang University.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 (5.1 µg/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Negative control : no staining on human kidney.
The section was incubated with ab211327 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of paraffin-embedded Human lung cancer tissue labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 (5.1 µg/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on human lung cancer.
The section was incubated with ab211327 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of formalin fixed paraffin embedded human small cell lung carcinoma labelling MASH1/Achaete-scute homolog 1 with ab211327 at a concentration of 0.1µg/ml. The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with a OptiView DAB IHC Detection Kit. Heat mediated antigen retrieval was performed with DISCOVERY cell conditioning solution (CC1) 100°C, pH8.5 for 32mins.
ab211327 Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] was incubated for 16mins at 37°C. Sections were counterstained with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.
Customers are encouraged to optimise antigen retrieval conditions, antibody concentration, incubation times and temperature for best results in their own IHC assay workflow (automated and manual)
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.5% Triton X-100 permeabilized NCI-H69 Human small cell lung cancer cells labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 dilution (red).
The nuclear counterstain is DAPI (blue).
Nuclear MASH1/Achaete-scute homolog 1 staining on NCI-H69 cells.
The images were kindly provided by our collaborator Dr. Hai Song, Zhejiang University.
- ChIP-seq
Lab
ChIP-sequencing - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Chromatin was prepared from NCI-H69 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab211327 [EPR19840]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- ChIP-seq
Lab
ChIP-sequencing - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Chromatin was prepared from NCI-H69 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab211327 [EPR19840]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- ChIP-seq
Lab
ChIP-sequencing - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Chromatin was prepared from NCI-H69 cells. Cells were fixed with 1% formaldehyde for 10 minutes. ChIP was performed with 107 cells and 8 µg of ab211327 [EPR19840]. ChIP DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 30 million reads. The input control is also shown.
- IP
Supplier Data
Immunoprecipitation - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
MASH1/Achaete-scute homolog 1 was immunoprecipitated from 0.35 mg of NCI-H69 (Human small cell lung cancer cell line) whole cell lysate with ab211327 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab211327 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10,000 dilution
Lane 1 : NCI-H69 whole cell lysate 10 μg (Input).
Lane 2 : ab211327 IP in NCI-H69 whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab211327 in NCI-H69 whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 minutes.
All lanes:
Immunoprecipitation - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327)
Predicted band size: 25 kDa
false
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 (5.1 µg/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Negative control : no staining on mouse kidney.
The section was incubated with ab211327 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of formalin fixed paraffin embedded mouse brain labelling MASH1/Achaete-scute homolog 1 with ab211327 at a concentration of 0.1µg/ml. The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with a ChromoMap DAB kit and anti-rabbit HQ and anti-HQ HRP detection. Heat mediated antigen retrieval was performed with DISCOVERY cell conditioning solution (CC1) 100°C, pH8.5 for 32mins.
ab211327 Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] was incubated for 16mins at 37°C. Sections were counterstained with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.
Customers are encouraged to optimise antigen retrieval conditions, antibody concentration, incubation times and temperature for best results in their own IHC assay workflow (automated and manual)
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 (5.1 µg/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on rat cerebrum.
The section was incubated with ab211327 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 (5.1 µg/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Negative control : no staining on rat kidney.
The section was incubated with ab211327 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
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-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of 4% paraformaldehyde-fixed mouse small cell lung cancer section labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 dilution, followed by Donkey anti Rabbit Alexa-594 at 1/500 dilution (red).
Nuclear counterstain : DAPI (blue).
Positive staining of MASH1/Achaete-scute homolog 1 on mouse small cell lung cancer.
The image was kindly provided by our collaborator Dr. Hai Song, Zhejiang University.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling MASH1/Achaete-scute homolog 1 with ab211327 at 1/100 (5.1 µg/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on mouse cerebrum.
The section was incubated with ab211327 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
MASH1/Achaete-scute homolog 1 was immunoprecipitated from 0.35 mg of mouse medullary thyroid cancer lysate with ab211327 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab211327 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10,000 dilution
Lane 1 : Mouse medullary thyroid cancer lysate 10 μg (Input).
Lane 2 : ab211327 IP in mouse medullary thyroid cancer lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab211327 in mouse medullary thyroid cancer lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 minutes.
All lanes:
Immunoprecipitation - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327)
Predicted band size: 25 kDa
false
- WB
Supplier Data
Western blot - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (AB211327)
Blocking/Dilution buffer : 5% NFDM/TBST.
Exposure time : Lane 1 : 15 seconds; Lane 2 : 10 seconds
Ascl1 is highly expressed in medullary thyroid cancer and small cell lung cancer (PMID : 17090547 and 25267614). Our results showed specific band on mouse medullary thyroid cancer lysate and NCI-H69 (Human small cell lung cancer) lysate. The lysates were kindly provided by our collaborator Dr. Hai Song, Zhejiang University.
All lanes:
Western blot - Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327) at 1/1000 dilution
Lane 1:
Mouse medullary thyroid cancer lysate at 20 µg
Lane 2:
NCI-H69 (Human small cell lung cancer cell line) whole cell lysate at 10 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: 25 kDa
Observed band size: 30 kDa
false
Related conjugates and formulations (1)
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Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] - BSA and Azide free
Reactivity data
Product details
Product Specifications
Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327) was developed by Abcam using patented rabbit monoclonal antibody technology and is validated for use in ChIP-seq, ICC/IF, IHC-P, IP, WB in human, mouse, rat samples.
Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327) specifically detects MASH1/Achaete-scute homolog 1 (UniProt ID: Q02067; Molecular weight: 25kDa) and is sold in 100 µL and 1 mL selling sizes.
Quality and Validation
Abcam's high quality manufacturing and validation processes ensure Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327) has high sensitivity and specificity alongside high lot-to-lot consistency and reproducibility.
Anti-MASH1/Achaete-scute homolog 1 antibody [EPR19840] (ab211327) has been cited over 21 times in peer reviewed journals and is trusted by the scientific community.
Related Products
Conjugation-ready, carrier free format available for antibody clone EPR19840 - ab240385.
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
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
This protein regulates the expression of genes important for the development of neuronal precursors. MASH1 does not act alone; it forms heterodimers with other bHLH proteins which enhance its ability to bind DNA and influence gene transcription. It helps convert multipotent neural progenitors into committed neuronal precursors which later differentiate into specific neuronal cell types. MASH1's role is particularly important during early stages of neuronal differentiation ensuring proper formation and maturation of the nervous system.
Pathways
MASH1 is central to the Notch signaling pathway and other pathways involved in neural differentiation. Within the Notch pathway MASH1 interacts with proteins like HES1 to balance the differentiation of neural progenitor cells into neurons and glial cells. This protein also connects with other pathway components such as NEUROG2 a downstream target to promote neuronal fate specification. These interactions illustrate MASH1’s integration into complex signaling networks that govern cell fate decisions during neurogenesis.
Product protocols
- Visit the General protocols
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Target data
Publications (49)
Recent publications for all applications. Explore the full list and refine your search
Nature 647:257-267 PubMed40963028
2025
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Molecular medicine (Cambridge, Mass.) 31:232 PubMed40500731
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Nature communications 16:4865 PubMed40419484
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Cancer immunology, immunotherapy : CII 74:213 PubMed40402312
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eLife 14: PubMed40388211
2025
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Cell reports 44:115597 PubMed40257863
2025
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Cells 14: PubMed40136675
2025
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EBioMedicine 112:105515 PubMed39808946
2025
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Proceedings of the National Academy of Sciences of the United States of America 121:e2405001121 PubMed39361648
2024
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Molecular cancer therapeutics 23:1789-1800 PubMed39295275
2024
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com