Name: ALX1 Lentiviral Activation Particles (m)
Brand: Molecular Depot
SKU: B2015380
Price: 995.00 USD
Availability: InStock

<h2 dir="ltr">What Is CRISPR/Cas9?</h2>
 CRISPR/Cas9 reagents are the guide RNAs, Cas9 proteins, and delivery components that enable precise, targeted edits to genomic DNA. They support knockout, knock-in, base editing, and gene regulation across cell lines, organoids, and model organisms. The quality directly affects editing efficiency, off-target activity, and experimental reproducibility. If your workflow involves genome engineering at a defined locus, there is a CRISPR/Cas9 reagent that applies.&nbsp; 
<h2 dir="ltr">What you will discover:</h2>
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<a href="https://mbpinc.net/reagents/gene-editing/crispr-cas9/mutation-detection-kits" title="Mutation Detection Kits:">Mutation Detection Kits:</a> Specialized enzyme-driven kits intended to measure the frequency of indel formation and confirm editing efficiency through T7E1 or Surveyor nuclease-mediated mismatch identification.
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<a href="https://mbpinc.net/reagents/gene-editing/crispr-cas9/cas9-enzymes" title="Cas9 Enzymes:">Cas9 Enzymes:</a> Nuclease-free Cas9, saCas9, and Cas12a (Cpf1) proteins of high purity equipped with NLS tags for swift translocation and precise double-strand break (DSB) induction.
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<a href="https://mbpinc.net/reagents/gene-editing/crispr-cas9/vector-and-lentivirus-systems" title="Vector and Lentivirus Systems:">Vector and Lentivirus Systems:</a>&nbsp;Enhanced transfection-quality dCas9 lentiviral systems fine-tuned for specific transcriptional activation (CRISPRa) or repression (CRISPRi) and enduring multi-omics integration.
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<a href="https://mbpinc.net/reagents/gene-editing/crispr-cas9/aav-adenovirus-systems" title="AAV/Adenovirus Systems:">AAV/Adenovirus Systems:</a> Optimized high-titer expression systems designed for effective AAV generation and temporary viral delivery, enabling tissue-targeted genomic alterations with components safe from endotoxins.
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<h2 dir="ltr">How to Choose CRISPR/Cas9 Reagents</h2>
 Cas9 Protein Variant Wild-type SpCas9 delivers high activity for standard knockout/knock-in. High-fidelity Cas9 reduces off-target editing. Nickase (Cas9n) supports paired-nick HDR strategies, dCas9 enables CRISPRa/CRISPRi gene regulation, and electroporation-ready RNP formats suit hard-to-transfect cells. Guide RNA Configuration Synthetic sgRNAs combine the target-specific spacer and scaffold in one molecule for convenience. Separate crRNA and tracrRNA components allow modular assembly and on-demand guide preparation for researchers needing flexibility. Delivery Format Plasmid delivery suits stable integration; RNP electroporation provides transient high-efficiency editing with a reduced genomic footprint; AAV and adenoviral vectors extend access to difficult-to-transfect primary cells and in vivo models. Post-Edit Validation T7 endonuclease I (T7E1)-based assays and alternative enzymatic mismatch cleavage kits detect insertions and deletions in edited cell populations. NGS-compatible workflows provide higher-resolution indel analysis where required. Application Scope CRISPR/Cas9 reagents support gene knockout and knock-in in mammalian cell lines, genome-modified animal model generation, functional genomics screens, and AAV/adenovirus-mediated in vivo delivery for gene therapy research. 
<h2 dir="ltr"> Specifications Context</h2>
 Key CRISPR/Cas9 specifications vary by reagent format and application. For nuclease proteins, researchers typically compare nuclease type (Cas9, saCas9, Cas12a/Cpf1), nuclear localization signal (NLS) configuration, protein format (liquid or lyophilized), and delivery compatibility. For viral delivery systems, vector type, viral titer, cargo capacity, and target cell compatibility are important considerations. Mutation detection kits are commonly evaluated based on assay sensitivity, workflow complexity, and compatibility with downstream analysis methods. Because genome editing workflows often combine nucleases, delivery systems, and validation reagents, researchers should confirm reagent compatibility, storage requirements, and experimental objectives before ordering. 
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<a href="https://mbpinc.net/contact-us" style="color: #236fa1;">Reach out to the MBP Inc. expert team</a> now to obtain a quote for the appropriate CRISPR/Cas9 reagents for your laboratory.

CRISPR/Cas9

Molecular Depot

Key Specifications

ALX1 Lentiviral Activation Particles (m)

ALX1 Lentiviral Activation Particles (m) by Molecular Depot is a preparation of lentiviral particles for the transcriptional activation of the ALX1 gene, designated m. Lentiviral delivery integrates the activation machinery into the genome of dividing and non-dividing cells alike, which is how a construct is introduced into cells that resist transfection. It is used to upregulate ALX1 expression in cells, in craniofacial development and neural crest research and in gene activation studies. Each unit contains 100 µL. MBP supplies Molecular Depot research reagents to research labs in the United States, Canada and worldwide.