Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Invitrogen iBlot Dry Blotting Gel Transfer System by Ethrog Biotechnologies is a laboratory instrument designed for dry transfer of proteins from gel matrices onto blotting membranes. This system utilizes a dry blotting transfer configuration to support protein transfer workflows commonly used in molecular biology and laboratory research applications. Its compact design provides an integrated platform for compatible gel transfer procedures without requiring a traditional wet transfer tank setup. Operating with a universal voltage input of 100–240V at 50/60Hz, this unit is suitable for compatible laboratory and research environments.
Specifications:
Brand: Invitrogen
Manufacturer / Distributor: Ethrog Biotechnologies
Product Name: iBlot
Product Type: Dry Blotting Gel Transfer System
Equipment Type: Laboratory Gel Transfer System
Transfer Type: Dry Transfer
Function: Protein Gel-to-Membrane Transfer
Voltage: 100–240V
Frequency: 50/60Hz
Application: Molecular Biology / Protein Analysis / Laboratory Research
Features:
Dry blotting transfer system configuration
Designed for protein gel transfer applications
Integrated laboratory transfer platform
Supports compatible blotting workflows
Universal 100–240V power input
50/60Hz frequency compatibility
Suitable for molecular biology research environments
Technical Details
| Brand | Invitrogen |
|---|---|
| Category | Dry Blotting Gel Transfer System |
| Medical Discipline | Biological Laboratory |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Ethrog Biotechnologies |
| SKU | DA451-ITEM-Q |
| Warranty | 30 - Warranty |
Need This Product Certified Patient-Ready?
If you require this product to be patient-ready certified, you can request a quote. Inspection, testing, repair, electrical safety testing, and calibration services are available through A Biomedical Service, Inc.
Related Products
No similar items available.
Safety & Biomedical Inspection Notice
Shipping & Receiving Notice
Medical equipment may require inspection, functional verification, calibration, preventive maintenance, safety testing, or other evaluations following transportation and before being placed into service.
Upon receipt, the purchaser is responsible for inspecting the equipment for any shipping damage and determining whether any inspection, testing, calibration, preventive maintenance, or certification is necessary based on the manufacturer's recommendations, the receiving facility's policies, and all applicable laws and regulations.
The equipment should not be placed into clinical service or used for patient care until the purchaser has verified that it is safe, appropriate, and compliant for its intended use.
Biomedical Inspection Notice
Medical equipment should be evaluated by qualified personnel before being placed into clinical service. Depending on the type of equipment, the evaluation may include, as applicable:
- Electrical safety testing
- Functional performance verification
- Alarm verification (if applicable)
- Battery inspection or replacement (if applicable)
- Calibration verification (if applicable)
- Preventive maintenance
- Software configuration and system settings
- Verification of compatible accessories, consumables, and disposables
- Inspection for shipping or handling damage
- Compliance with the manufacturer's recommendations
- Compliance with the receiving facility's policies, procedures, and applicable regulatory requirements
Transportation, storage, handling, and installation may affect the performance of medical equipment. Reuse Medical recommends that the receiving facility inspect, test, and evaluate the equipment in accordance with the manufacturer's recommendations and the facility's biomedical engineering procedures before placing the equipment into clinical service or patient use.
