| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | Asparagine synthetase [glutamine-hydrolyzing];6.3.5.4;Cell cycle control protein TS11;Glutamine-dependent asparagine synthetase;ASNS;TS11; |
| Cellular Localization | |
| Clonality | |
| Concentration | |
| Form | Liquid |
| Host | |
| Immunogen | A synthesized peptide derived from human SMARCC1/BAF155 |
| Isotype | |
| Molecular Weight | |
| Product Type | |
| Reactivity | |
| Reconstitution | |
| Storage | |
| Target | |
| UniProt # |
Overview
This product is an anti-SMARCC1 antibody for target detection and characterization. Key identifiers include host species: Rabbit; Monoclonal; clone 18S70; isotype IgG; reactivity: Human,Rat. Reported application contexts include WB, ICC, IF, IP, Flow (as provided in the source record). Boster Bio Anti-SMARCC1/BAF155 Rabbit Monoclonal Antibody catalog # M03303-1. Tested in WB, ICC/IF, IP, Flow Cytometry applications. This antibody reacts with Human, Rat.
Key elements and design rationale
- Target: SMARCC1 (Asparagine synthetase [glutamine-hydrolyzing]).
- Antibody format: Monoclonal; clone 18S70; isotype IgG.
- Host: Rabbit.
- Species reactivity: Human,Rat (confirm in your model system with appropriate controls).
This description is intended to help interpret the antibody design and the biological context of the target using the fields provided in the catalog record, alongside general experimental considerations.
Biological background
SMARCC1 (protein: T-cell surface glycoprotein CD3 zeta chain) is a commonly studied target in molecular and cellular biology. Functional context (as provided): Acts as an intracellular estrogen-binding protein. May be involved in modulating cellular levels and biological functions of estrogens in the pancreas. May act as a chaperone that inhibits aggregation of misfolded proteins. . Reported cellular localization context: Endoplasmic reticulum lumen . Tissue expression notes (as provided): Highly expressed in pancreas (at protein level). .
Research relevance and current trends
- Research context keywords from the source record include: Amino Acid Metabolism,Amino Acids,Cancer,Metabolic Signaling Pathways,Metabolism,Pathways and Processes,Signal Transduction.
- Current studies often focus on connecting target abundance/localization to pathway perturbations across models, tissues, and cell states.
- Quantitative and multiplexed assays (e.g., imaging + immunoblot panels) are commonly used to compare phenotypes across conditions and time-courses.
Common research applications
- Western blotting (WB): assess relative target abundance across samples, treatments, or time-points.
- Immunofluorescence/ICC (IF/ICC): visualize subcellular localization patterns and cell-to-cell heterogeneity.
- Flow cytometry: quantify target-positive populations and compare shifts in marker distributions.
- Immunoprecipitation (IP): enrich target complexes for downstream immunoblot or interaction analyses.
Workflow ideas (metafield): Validate SMARCC1 antibody specificity using KO/KD control samples (WB/IF/IHC as appropriate), Detect SMARCC1 expression by Western blot in cell or tissue lysates, Localize SMARCC1 by immunofluorescence/immunocytochemistry in cultured cells, Quantify SMARCC1-positive cells by flow cytometry in single-cell suspensions, Enrich SMARCC1 by immunoprecipitation from lysates for downstream analysis
Notes for experimental interpretation
- Consider isoforms and post-translational modifications (PTMs) that may shift apparent molecular weight or epitope accessibility.
- Apparent molecular weight may vary by sample type and processing (observed MW: 18 kDa; calculated MW: 64370 MW).
- Control concepts: include appropriate negative controls (e.g., isotype, KO/KD samples) and orthogonal validation when feasible.
Additional product details (from the source record)
- Molecular weight (observed): 18 kDa
- Cellular localization (provided): Endoplasmic reticulum lumen .
- Tissue details (provided): Highly expressed in pancreas (at protein level). .
Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.
