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3α -Hydroxysteriod Dehydrogenase Hsd Diagnostic Enzyme White Freeze-Dried Powder
Negotiable
100 KU
Product profile
Customization
AvailableCAS No.
NoFormula
NoModel NO.
HSDEINECS
NoClassification
Biological AgentsGrade
ARSpecific Usage
For Biological PurposeContent
StandardUsage
Laboratory Reagents, Analytical Reagents, Diagnostic ReagentsSource
CompositionHabit Appellation
HsdApplication
Scientific Research, HealthProperty
Biochemical ReagentStorage
Low Temperature StorageUse to
in Vitro Diagnostic KitManufactor
Hubei New Desheng Material Technology Co., LtdDosage Form
White Freeze-Dried PowderTransport Package
Refrigerated TransportSpecification
10mg/bottleTrademark
DeShengOrigin
Ezhou City, Hubei Province, ChinaProduction Capacity
50g Per MonthKey features
Critical Diagnostic Role: Serves as the first-step enzyme in sialic acid detection kits for monitoring malignant tumors.
Trinder Reaction Compatible: Designed for use in Trinder reaction-based diagnostic kits for uric acid, cholesterol, and glucose.
Manufacturer Direct Supply: Produced by Hubei New Desheng, a specialized manufacturer with 9 R&D engineers and advanced equipment.
Customization Available: OEM and ODM services are available, allowing customization from samples for specific needs.
Fast Lead Time: Average lead time is within 15 workdays for both peak and off-season periods.
Strict Quality Control: Features 3 QA/QC inspectors and random inspection for finished products to ensure consistency.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples CertifiedExport Year: 7 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤5.95h
AI-Powered supplier vetting
SummaryThe supplier is a combined manufacturing and trading enterprise with chemical, synthetic-material, medical-device, and related product activities. It reports two production lines, specified annual capacities for several products, finished-product inspection instructions, inventory capability, and an off-peak lead time within 15 working days. Service processes for corrective and preventive actions and customer complaints are documented and followed. R&D personnel provide technical support, with design and verification records available for audit, but no SDK is available. The supplier provides OEM services for well-known brands and can customize from samples. Limitations include no valid manufacturing-capacity contract with related subcontractors, no overseas warehouse, showroom, agent, or branch, and no stated overseas service countries. No explicit certification holdings or customer case details are provided.
Supplier typeThe supplier’s stated scope covers manufacturing of basic chemical raw materials, synthetic and bio-based materials, special chemical products, sealing fillers, engineering plastics, and Category I and Category II medical-device sales. It is identified as a combined company rather than an offshore company, indicating a mixed manufacturing and commercial operating model.
After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions and customer complaints, and technology engineers provide technical support for production and after-sales service. However, it reports no overseas agents or branches, no overseas warehouse or showroom, and zero stated countries for overseas services, limiting evidence of local international support.
R&D capabilityR&D engineers are responsible for R&D and technical support, and relevant design input, output, review, verification, and validation documents are available for audit. The supplier reports software-instrument capability using MestReNova, but no SDK is available, so the evidence supports established R&D activity rather than full software-development integration capability.
Production capacityThe supplier operates two production lines and reports defined annual capacities, including 600 tons of serum separation gel, 500 tons of tris base, 30 tons of dipotassium ethylenediaminetetraacetate, 20 tons of tripotassium EDTA, and 0.6 tons of lithium heparin. It also reports inventory capability, standardized finished-product inspection instructions, and an off-peak lead time within 15 working days; however, it lacks a valid manufacturing-capacity contract with related subcontractors.
Customization capabilityThe supplier explicitly offers design customization from samples and reports OEM services for well-known brands. Its quality-control information also states that own-brand product quality-control capability is present, although the specific designation is recorded as “DS.”
Product Q&A
Q:What is the main application of this enzyme?
A:
It is primarily used as a key component in in vitro diagnostic reagent kits, specifically for the enzymatic detection of sialic acid to monitor malignant tumors.
Q:Is customization available for this product?
A:
Yes, OEM and ODM services are available. Customization can be done from samples.
Q:What is the minimum order quantity (MOQ)?
A:
The minimum order quantity is 100kgs.
Q:What are the payment terms?
A:
We accept LC, T/T, PayPal, Western Union, and small-amount payments.
Q:What is the lead time for delivery?
A:
The average lead time is within 15 workdays, regardless of peak or off-season.
Send Inquiry
*To:
Hubei New Desheng Material Technology Co., Ltd
Hubei New Desheng Material Technology Co., Ltd*Content:
Supplier replies will be sent to your registered email
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