Arrayed gRNA Libraries

March 5, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Arrayed gRNA Libraries

Smarter, Faster, and More Efficient CRISPR Screening

Achieve unparalleled knockout efficiency with EditCo’s multi-guide CRISPR design. Our Arrayed CRISPR gRNA Libraries eliminate the inefficiencies of traditional loss-of-function screens, offering a reliable and ready-to-transfect solution. With up to three spatially coordinated sgRNAs per gene, our approach ensures higher knockout success, reduces false negatives, and eliminates the need for complex NGS data analysis. Designed for both human and mouse genes, our libraries provide fast delivery, robust quality control, and seamless Sanger sequencing analysis—so you can focus on results, not troubleshooting.

Whole Genome CRISPR Libraries for Comprehensive Gene Editing

EditCo’s Whole Human and Whole Mouse Genome Libraries provide unmatched gene coverage with our multi-guide design, ensuring high editing efficiency across 20,000+ gene targets. Designed for seamless transfection, these libraries reduce false negatives and eliminate time-consuming preparation, making large-scale CRISPR screening easier than ever.

– Comprehensive Coverage: Target the entire human or mouse genome with high knockout efficiency.
– Ready-to-Use Libraries: Pre-plated and transfection-ready, minimizing preparation time.
– Enhanced Stability: Chemically modified sgRNAs resist degradation and prevent immune responses.
– Flexible Formats: Available in 96- or 384-well plates with multi-guide sgRNAs for reliable gene disruption.

Accelerate Target Discovery with Pathway Libraries

EditCo’s 30+ Pathway Libraries, including druggable targets, GPCRs, kinases, and immuno-oncology genes, provide a powerful tool for target identification studies. Designed with our multi-guide CRISPR strategy, these libraries ensure high knockout efficiency and fewer false negatives. Select libraries ship in as little as one week, helping you start your screen faster.

– Diverse Pathway Coverage: Includes key gene sets for drug discovery and functional studies.
– Fast Shipping: Select libraries ready to ship within a week.
– High-Efficiency Knockouts: Multi-guide sgRNAs deliver precise, predictable gene disruption.
– Ready-to-Use Format: Available in 96- or 384-well plates with modified sgRNAs for stability.

Available Gene Pathways

Optimal Knockout Efficiency for High-Throughput Screening

XDel technology delivers precise, high-efficiency knockouts by using a multi-guide RNA strategy that ensures consistent and reliable gene editing. Unlike traditional single-guide methods, XDel induces fragment deletions in early exons, maximizing on-target accuracy while minimizing variability and off-target effects.

Superior editing efficiency – Multi-guide design achieves higher and more consistent knockouts
Reduced off-target effects – XDel minimizes unintended edits compared to single-guide methods
Sustained knockout effects – Gene edits remain stable across multiple cell passages
High viability & protein depletion – Maintains cell health while ensuring effective functional knockouts

Achieve robust genotype and phenotype screening with XDel’s optimized CRISPR knockout technology.

Image: XDel multiple gRNA creates fragment deletions

Image: XDel design includes up to 3 modified sgRNAs (grey bars) that target a single gene of interest

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Ready to Order?

Gene Knockout kits

Arrayed gRNA Libraries

Let’s Find You an Application That Helps Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Gene Knockout Kits

March 4, 2025/in EditCo, Partners/by Harshita Sharma

EditCo Gene Knockout Kits: Reliable and Efficient CRISPR Solutions

EditCo’s Gene Knockout Kit offers a simplified, highly efficient solution for generating human and mouse protein-coding gene knockouts.

Unlike traditional CRISPR methods, which rely on a single guide RNA (gRNA) to create random indels, EditCo’s multi-guide approach ensures consistent and precise gene disruption. This method generates fragment deletions at the targeted loci, providing a more reliable and predictable knockout, ultimately enhancing experimental success.

With fast delivery times (kits arrive in just 5 days), users can avoid the trial and error of guide screening and proceed quickly with their experiments. The process is streamlined further with an easy online ordering portal, which includes the option to purchase controls, SpCas9 nuclease, and Transfection Optimization kits to complement your knockout experiment.

This solution guarantees high knockout efficiency, making gene editing faster and more reliable than ever before.

Why It Matters

Maximise Gene Disruption

XDel’s multi-guide CRISPR design consistently delivers higher on-target editing across multiple loci and cell types. By coordinating 2–3 sgRNAs per exon, researchers can achieve complete functional knockouts with minimal variability.

Precision Editing with Minimal Risk

Off-target edits are a major concern in gene editing. XDel’s cooperative guide approach allows for lower gRNA concentrations while maintaining efficiency, reducing unintended edits and improving experimental reliability.

Persistent Protein Depletion, Straight to Assays

Edited cell pools maintain stable protein loss for weeks, enabling direct use in downstream functional assays. This reduces validation cycles and accelerates your research timelines.

Why Traditional Knockouts Fall Short

Despite its power, CRISPR-Cas9 isn’t foolproof. Most conventional knockout strategies rely on a single guide RNA to induce a small insertion or deletion (indel) at the target site. In theory, this should disrupt the reading frame and deactivate the gene — but in practice, it rarely works that cleanly.

Even minor indels can restore partial functionality or trigger alternative splicing, leaving residual protein activity that undermines downstream results. What should be a “complete knockout” often ends up a mosaic of mixed edits, forcing researchers to spend additional time validating, recloning, or repeating experiments.

And it doesn’t stop there — when working with complex or sensitive cell models like iPSCs, low editing efficiency and variable expression recovery make reproducibility a constant battle. The result? Weeks lost, inconsistent phenotypes, and data that’s difficult to interpret or publish.

Researchers need more than chance-based gene disruption.
They need an approach that targets with precision, edits consistently across cell types, and produces true functional knockouts the first time.

That’s exactly where XDel Technology steps in.

XDel Technology – Coordinated, Multi-Guide Editing

Traditional CRISPR depends on a single cut — a gamble on where repair enzymes will introduce small, random indels. XDel takes a fundamentally smarter approach.

Instead of one guide, XDel uses up to three sgRNAs targeting sites within the same exon. These guides work together to generate coordinated fragment deletions, ensuring the targeted region is fully removed rather than partially disrupted. The result is a true functional knockout — not a mixture of partial edits.

This multi-guide design provides several key advantages:

Higher knockout efficiency: Coordinated cuts increase the likelihood of complete loss of gene function across all alleles.
Cleaner edit outcomes: Large, predictable deletions are easier to confirm with standard PCR or sequencing, reducing downstream validation time.
Compatibility across cell types: Proven performance in immortalized, primary, and iPSC models — even those typically resistant to editing.

By shifting from random indels to engineered deletions, XDel dramatically improves experimental reproducibility and shortens the path from edit design to verified knockout.

Whether your work is in functional genomics, disease modeling, or drug discovery, XDel technology helps you achieve reproducible results faster and with less rework. Decode Science is the official Australian distributor of EditCo. So feel free to reach out to me if you have any questions.

Data-Proven Performance

XDel isn’t theory — it’s backed by real, quantitative data across multiple loci and cell types.

In comparative studies of seven endogenous genes across four different cell lines, XDel’s multi-guide approach consistently outperformed conventional single-guide designs in both knockout efficiency and edit consistency.

1. Higher and More Consistent On-Target Editing

Traditional single-guide methods introduce random indels that often yield partial or incomplete knockouts.
XDel solves this by deploying up to three predesigned sgRNAs targeting a single exon, working together to generate large fragment deletions.
Across seven endogenous loci in four cell lines, this approach achieved significantly higher and more consistent editing efficiencies — reducing the rework often required in CRISPR experiments.

2. Stable Protein Depletion Across Time

Effective gene disruption means sustained loss of protein function, not just transient edits.
In K562 cells, XDel-mediated knockouts of four membrane proteins maintained stable protein depletion for up to 21 days post-editing — with >90% cell viability throughout.
These pools are immediately assay-ready, eliminating the need for additional validation or re-editing.

Click on image to view full size

3. Fewer Off-Target Edits, Greater Precision

A key concern with multi-guide systems is off-target activity — but XDel’s design delivers the opposite.
Rigorous NGS analysis across 63 off-target loci confirmed that XDel edits are more precise than single-guide approaches, showing markedly lower off-target frequencies across both immortalized and iPSC lines.

4. Confirmed Protein Knockout Across Multiple Genes

Western blot analyses for five independent target genes confirmed complete and consistent protein depletion at days 7, 14, and 21 post-transfection.
This demonstrates that XDel doesn’t just produce edits — it reliably eliminates functional protein expression across diverse gene targets.

5. High Editing Efficiency at Lower gRNA Concentrations

The cooperative behavior of XDel’s multi-guide system enables lower total gRNA usage while maintaining exceptional on-target editing rates.
Even when RNP concentrations were reduced to 0.25×, editing remained high with minimal off-target impact — translating to more cost-efficient and cleaner edits.

Applications Across Research Areas

Functional Genomics

Disease Modeling

Drug Discovery and Target Validation

CRISPR Screening and High-Throughput Studies

Talk to Our Specialist

Decode Science is the official distributor of EditCo in Australia and New Zealand, helping researchers access XDel Knockout Technology with local expertise and technical support. Our team works alongside you to identify the right solutions for your workflow — from targeted knockouts to large-scale CRISPR screens — backed by EditCo’s proven data and Decode’s commitment to reproducibility.

For more information or project-specific guidance, reach out to Hamza Hassan, our business development manager, to discuss how XDel can accelerate your next experiment.

CRISPR Reagents Portfolio

Gene Knockout kits

Arrayed gRNA Libraries

Knockout T-cells

March 4, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knockout CD8+ & CD4+ T Cells

Advanced CRISPR Knock-Ins for iPSC Research

EditCo delivers efficient gene editing with guaranteed >80% efficiency in human primary cells, achieving >90% in many cases, using a smart multi-guide design and a 7-day protocol for results in 2 weeks or faster. Their Primary Cell KO Pools produce functionally consistent cell populations, ideal for drug discovery or biological modeling, while maintaining high viability and functionality. Researchers can use EditCo-supplied cells or their own CD8+/CD4+ T cells, ensuring flexibility and reliability. By minimizing failed experiments and false negatives, EditCo saves time and resources, offering 1M-cell EC Pools for high-quality, rapid, and dependable gene editing.

Image: High editing efficiency across multiple donors.

Image: EditCo KO CD8+ T cell pools can be thawed and expanded for weeks, with or without TCR stimulation.

Next-Level Edited CD8+ T Cells – Powerful, Stable, and Ready for Action

Take your research further with precision-engineered CD8+ T cells that combine high editing efficiency, long-term stability, and exceptional functionality. Designed to maintain their knockout integrity, expand effortlessly post-thaw, and deliver strong antigen-specific responses, these cells are built for performance. Whether you’re exploring immune responses or advancing cell therapy, these edited T cell pools provide the reliability and power you need.

🔬 Unmatched Editing Precision – Achieve over 90% knockout efficiency across multiple donors, maintaining stability before and after cryopreservation.

🧬 Thrives & Expands with Ease – These cells stay healthy and proliferate for weeks, with or without stimulation, ensuring flexibility in your experiments.

⚡ Optimized for Real-World Function – A single round of activation preserves normal function, preventing overstimulation and exhaustion.

🎯 Potent, Targeted Cytotoxicity – Strong antigen-specific activation, with robust CD107a expression, ensures effective tumor-killing potential.

Power up your research with CD8+ T cells engineered to perform when it matters most.

CD4+ T Cells - Stability and Functionality Post-Editing

The editing of CD4+ T cells has shown high efficiency and stability, with a robust ability to maintain functionality after the editing process. The efficiency of the CD4+ T cell editing was determined through ICE analysis, with results demonstrating high editing efficacy across multiple loci while ensuring cell viability during the freezing stage. Post-editing, the cells can be thawed and expanded without loss of functionality or editing efficiency. Cytokine production in edited T cells, including IFNg, IL2, and TNFa, indicates that the editing process does not negatively impact the cells’ ability to produce essential cytokines upon stimulation. These edited pools also show high viability, making them suitable for further downstream assays.

– High editing efficiency of CD4+ T cells determined by ICE analysis.
– No reduction in cell viability after freezing, as indicated by flow cytometry
– Successful expansion and thawing of edited cells without affecting functionality
– Edited cells exhibit high levels of cytokine production (IFNg, IL2, TNFa) post-stimulation
– High viability and expansion potential, with >90% viability after 14 days in culture
– Statistical analysis shows significant cytokine differences between edited and mock cells

Image: Editing Efficiency and Viability for CD4+ T cell pools.

Image: Editing Efficiency leads to protein depletion as shown by flow cytometry

Image: CD4+ pool stability after thaw.

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

Let’s Find You an Application That Helps Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Knockout Immortalized Cells

February 28, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knockout Immortalized Cells

Reliable, Reproducible CRISPR Editing for Breakthrough Discoveries

Spend Less Time on Editing, More on Innovation: EditCo’s advanced automation eliminates time-consuming steps, allowing you to focus on impactful research.

Superior Performance & Scalability: Our CRISPR platform delivers high knockout efficiencies, ensuring consistent, reproducible results across experiments.

XDel Knockout Cell Pools & Clones

XDel is an advanced CRISPR knockout tool that eliminates uncertainty in gene editing. Using a groundbreaking guide RNA design approach, it provides highly effective, reliable, and repeatable gene knockouts, enabling researchers to speed up their breakthroughs with assurance.

– Higher Efficiency & Consistency: XDel technology ensures superior on-target knockout rates with minimal variability.
– Reduced Off-Target Effects: Achieve precise edits with lower unintended mutations compared to single-guide methods.
– Validated & Scalable: Persistent protein depletion enables direct use in functional assays, drug discovery, and disease modeling.

CRISPR Knockout Cell Pools & Clones

Accelerate your research with high-efficiency CRISPR Knockout Cell Pools & Clones from EditCo. Our cell pools provide a mix of edited and unedited cells for immediate assays, while clonal lines ensure precise gene knockouts with sequence-verified accuracy.

– 50%+ knockout efficiency in cell pools
– Up to 95% protein knockout for functional validation
– Single, double, or triple knockouts available
– Comprehensive QC & sequencing reports included

Knockout Cell Libraries – High-Throughput CRISPR Screening Made Easy

EditCo’s Knockout Cell Libraries enable high-efficiency CRISPR screening with over 90% editing success in a ready-to-use 96-well arrayed format. Designed for functional assays and drug target discovery, our libraries eliminate transfection challenges and infrastructure barriers.

– Multi-guide CRISPR design for precise knockouts
– High-throughput screening with scalable workflows
– Comprehensive QC & sequencing reports included
– Compatible with diverse assays for discovery & validation

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

Immortalized Cells Portfolio

Knockout Immortalized Cells

Knock-in Immortalized Cells

Let’s Find You an Application That Helps Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Knock-in iPS Cells

February 28, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knock-in iPS Cells

Advanced CRISPR Knock-Ins for iPSC Research

EditCo’s advanced CRISPR knock-ins empower neuroscience, cardiovascular, and regenerative medicine research by delivering precise edits in iPSCs while maintaining their quality, pluripotency, and integrity. Our high-throughput automated platform ensures fast lead times and high editing efficiencies, allowing you to focus on downstream applications like assay development and differentiation.

With minimal off-target effects, our platform offers a range of knock-ins, including single nucleotide variants, tags, and small insertions (<100 bp), available in both homozygous and heterozygous states, as well as in clone or pool formats. Trust EditCo’s robust editing process to accelerate your discoveries with artifact-free, reliable CRISPR-edited iPSCs.

Image: iPS cells were assessed for standard pluripotency markers, three days post-editing.

Single-guide RNA Knock-in Cell Pools

Achieve high-efficiency CRISPR iPSC knock-ins with EditCo’s Knock-in iPS Cell Pools. These pools offer a mix of edited and unedited cells, giving you flexibility for clonal isolation. Our optimized platform ensures precise edits, while you have the option to perform clonal isolation yourself. For those looking for a fully automated process, explore our Knock-in iPS Cell Clones for homogeneity and convenience.

Features:

– Cell Source: EditCo or customer supplied
– Available Edits: SNV, Tag, or Insertion
– CRISPR Design: Synthetic modified sgRNA, Donor ssODN
– Add-ons: QC for pluripotency testing

Deliverables:

– Edited cell pools (2 vials with 5 million cells)
– Regular updates, sequencing data, and comprehensive QC reports

EditCo ensures robust editing with high efficiency across a variety of iPSC lines, maintaining pluripotency and delivering consistent, reliable results.

Single-guide RNA Knock-in Cell Clones

EditCo’s Knock-in iPS Cell Clones provide homogeneous populations derived from single CRISPR-edited cells. Skip the editing and cloning process, and move directly into functional assays with high-quality, reliable clones. We manage the entire CRISPR editing and cloning process, ensuring you receive precise, genetically modified clones for accelerated research.

Features:

– Cell Source: EditCo or customer supplied
– Genetic Modifications: SNV, Tag, or Insertion (Homozygous or Heterozygous)
– CRISPR Design: Synthetic modified sgRNA, Donor ssODN
– Add-ons: Additional clones, QC for pluripotency and karyotype testing

Deliverables:

– 2 independent clones with the required knock-in (2 vials of 500,000 cells each)
– Regular progress updates, sequencing data, and comprehensive QC reports

EditCo ensures precise SNV editing and delivers reliable, pluripotent clones ready for your downstream applications.

Image: 100% SNV editing in iPS cell clones.

Use EditCo’s iPS Cell Lines or Bring Your Own
EditCo provides iPS cell lines for all engineered cell orders at no extra cost. Alternatively, you can onboard your own cell lines.

* Parental vials available for evaluation prior to booking an edit

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

IPS Cells Portfolio

Knockout iPS Cells

Knock-in iPS Cells

Let’s Find You an Application That Helps Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Knockout iPS Cells

February 28, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knockout iPS Cells

Precise and efficient models for cutting-edge disease research.

EditCo’s cutting-edge CRISPR technology ensures accurate and efficient gene editing while maintaining iPSC quality, pluripotency, and overall cell integrity. Our automated platform, optimized guide design, and superior reagents enable high-efficiency knock-ins and knockouts, minimizing errors and off-target effects. With a focus on delivering reliable and functional gene modifications, our robust process allows researchers to confidently assay gene functions, model diseases, and explore new therapeutic targets.

Whether you need precise knockouts or complex knock-ins, EditCo’s advanced editing solutions provide the accuracy and consistency required for high-impact scientific discoveries in biomedical research.

XDel Knockout Cell Pools and Clones

XDel is a CRISPR technology for precise, efficient gene editing. With a unique guide RNA design, it ensures reproducible knockouts without affecting pluripotency or cell integrity, accelerating research in gene function, disease modeling, and drug development.

– High Efficiency: Superior editing and consistent knockouts.
– Reliable Results: Persistent protein depletion validated through assays.
– Reproducibility: Minimized variability for dependable outcomes.

Features

– Cell Source: EditCo or customer supplied.
– Available Edits: Indel, fragment deletion, homozygous, or heterozygous.
– Design: Synthetic modified sgRNA.
– Add-Ons: Additional clones, testing.
– Deliverables: Updates, edited cell pools (2 vials), sequencing data, and QC reports.

Superior Editing
XDel offers more consistent and efficient on-target editing than single-guide RNA methods, ensuring reliable results.

Reduced Off-Target Effects
XDel delivers lower off-target editing compared to single-guide RNA, ensuring better precision.

Robust Knockouts
XDel pools maintain genomic stability, confirmed by karyotyping and PluriTest™.

How XDel Works
XDel uses up to 3 coordinated guides for reliable knockouts, offering more consistent edits than traditional single-guide methods.

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

IPS Cells Portfolio

Knockout iPS Cells

Knock-in iPS Cells

Let’s Find You an Application That Helps Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Knock-in Immortalized Cells

February 27, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knock-in Immortalized Cells

Get CRISPR-Engineered Cell Lines Faster and More Efficiently.

EditCo’s Knock-in Immortalized Cells provide a fast and efficient way to integrate engineered cells into your research, using automated transfection optimization and RNP-based delivery to ensure high editing success with minimal off-target effects.

By eliminating the delays and challenges of DIY CRISPR projects, our cost-effective solution enables you to model more genes and variants across multiple cell lines, accelerating your path to discovery without overspending.

Cost-Effective CRISPR Knock-in Cell Pools – Flexible & Efficient

EditCo’s Knock-in Immortalized Cell Pools provide a high-throughput, budget-friendly solution for introducing precise edits while maintaining a mixed population of edited and unedited cells.

– Optimized transfection for high-efficiency knock-ins
– Supports SNVs, tags, and large insertions with advanced HDR strategies
– Flexible clonal isolation—manage it yourself or opt for our Knock-in Clones
– Comprehensive QC & sequencing reports for reliable validation

Precision-Verified CRISPR Knock-in Clones – Ready for Your Research

EditCo’s Knock-in Immortalized Cell Clones provide a sequence-verified, clonal population for precise, high-quality knock-ins. Whether modifying SNVs, tagging proteins, or inserting large sequences, our automated isolation process ensures you receive a single-cell-derived clone with your desired edit.

– Guaranteed precision with fully validated knock-ins
– Endogenous tagging & SNV editing for functional studies
– Streamlined delivery with complete QC & sequencing reports
– Customizable options including additional clones & intermediate pools

Skip the complexity—get ready-to-use, precision-edited clones with EditCo!

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

Immortalized Cells Portfolio

Knockout Immortalized Cells

Knock-in Immortalized Cells

Let’s Find You an Application That Helps Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Arrayed gRNA Libraries

Smarter, Faster, and More Efficient CRISPR Screening

Let’s Find You an Application That Helps Your Research

EditCo Gene Knockout Kits: Reliable and Efficient CRISPR Solutions

Maximise Gene Disruption

Precision Editing with Minimal Risk

Persistent Protein Depletion, Straight to Assays

Hamza Hassan

Functional Genomics

Disease Modeling

Drug Discovery and Target Validation

CRISPR Screening and High-Throughput Studies

Knockout CD8+ & CD4+ T Cells

Advanced CRISPR Knock-Ins for iPSC Research

Focus on your experiment while they handle CRISPR

Choose your starting point

Transparent and detailed results

Reliable and validated outcomes

Let’s Find You an Application That Helps Your Research

Knockout Immortalized Cells

Reliable, Reproducible CRISPR Editing for Breakthrough Discoveries

Characterize Genes Associated with Neurodegenerative Disease:

Investigate a Protein’s Mechanism of Action:

Expedite Drug Discovery Research:

Thoroughly Confirm Your Phenotype in Multiple Models in Parallel:

Let’s Find You an Application That Helps Your Research

Knock-in iPS Cells

Advanced CRISPR Knock-Ins for iPSC Research

Isogenic Neuronal Lines:

Drug Screening:

Protein Tagging:

Disease Modeling:

Let’s Find You an Application That Helps Your Research

Knockout iPS Cells

Precise and efficient models for cutting-edge disease research.

Gene Function Studies:

Gene-Disease Linkage:

Pathway Analysis:

Target Validation:

Let’s Find You an Application That Helps Your Research

Knock-in Immortalized Cells

Get CRISPR-Engineered Cell Lines Faster and More Efficiently.

Tag and Quantify Your Protein:

Create a Disease Model:

Analyze Gene Regulation:

Uncover Protein Interactions:

Let’s Find You an Application That Helps Your Research

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Instant Download

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Special October Offer

FREE UMBRELLA

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