Polyclonal Antibodies
KO Validated Anti-Smad1 Rabbit Polyclonal Antibody for WB, IHC-P, IF/ICC, ELISA - Q15797
Item Number : CM0023723
Price varies based on specs and customizations
- Application
- WB, IHC-P, IF/ICC, ELISA
- Cross Reactivity
- Human, Mouse, Rat
- Protein Weight
- 52kDa
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Core Product Specifications and Parameters
| Parameter | Value |
|---|---|
| Product Name | [KO Validated] Smad1 Rabbit pAb |
| Remarks/Alias | BSP1; JV41; BSP-1; JV4-1; MADH1; MADR1; d1 |
| Species | Human |
| Gene ID (Human) | 4086 |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 20-240 of human Smad1 (NP_001003688.1) |
| Source | Rabbit |
| Category | Polyclonal Antibodies |
| Application | WB, IHC-P, IF/ICC, ELISA |
| Cross Reactivity | Human, Mouse, Rat |
| SWISS | Q15797 |
| Protein Weight | 52kDa |
| Shipping | Ice bag |
Biological Background: Smad1 Function and Localization
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Protein identity: SMAD family member 1 (Smad1), also known as BSP-1, JV4-1, MADH1, MADR1. Functions as a transcriptional modulator in embryonic development, cell differentiation, and tissue homeostasis. Related references: PMID:9335504
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Upon BMP ligand binding, Smad1 is phosphorylated by activated type I BMP receptors, then associates with SMAD4 to form a heteromeric complex that translocates to the nucleus and acts as a transcription factor. Related references: PMID:33667543
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The nuclear Smad1/SMAD4 complex recognizes cis-regulatory elements containing Smad Binding Elements (SBEs) to modulate gene expression. Related references: PMID:33667543
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Smad1, in complex with OAZ1 and PSMB4, mediates the degradation of the CREBBP/EP300 repressor SNIP1, linking BMP signaling to transcriptional coactivator regulation.
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Smad1 positively regulates BMP4-induced expression of the odontogenic development regulator MSX1 following IPO7-mediated nuclear import.
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Subcellular localization is both cytoplasmic and nuclear, consistent with its role in signal transduction from the cell membrane to the nucleus.
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Tissue expression is ubiquitous, with highest levels observed in heart and skeletal muscle.
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Post-translational modifications include phosphorylation, acetylation, and ubiquitination; it contains a zinc-binding domain and functions as a DNA-binding transcription factor.
Experimental Guidance and Technical Tips
- Based on the immunogen design (amino acids 20-240 of human Smad1), the antibody may recognize both unphosphorylated and phosphorylated forms; consider assessing phospho-specificity with appropriate controls.
- For Western blot, an expected band at approximately 52 kDa should be observed; use tissue or cell lysates with high Smad1 expression (e.g., heart or skeletal muscle) as positive controls.
- KO validation suggests suitability for confirming target specificity in knockout cell lines or tissues; include a wild-type control where possible.
- For IHC-P and IF/ICC, optimize antigen retrieval and antibody dilution using known positive tissue samples; cross-reactivity with mouse and rat allows use in rodent models.
- As a polyclonal antibody, lot-to-lot consistency may vary; validate each new batch in the intended application and always include appropriate controls.
CamelBio: Your One-Stop Sourcing Bridge
CamelBio provides diagnostic manufacturers, labs, and research institutes with one-stop access to IVD raw materials, technical services, and consulting—covering every stage from concept to clinic. For BMP signaling and transcription regulation research, we offer validated antibody pairs, optimized monoclonal/polyclonal antibodies like this anti-Smad1 antibody, and bulk ancillary reagents to support your assay development. Our team can also assist with rare target raw-material sourcing, ensuring you have a reliable supply chain from target identification to final product.
Product Datasheet
KO Validated Anti-Smad1 Rabbit Polyclonal Antibody for WB, IHC-P, IF/ICC, ELISA - Q15797
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