MT35030CV

Corning™ Donor Horse Serum, U.S. Sourced

Manufacturer: Corning™

Select a Size

Pack Size SKU Availability Price
Each of 1 MT35030CV-Each-of-1 In Stock ₹ 30,074.34

MT35030CV - Each of 1

₹ 30,074.34

In Stock

Quantity

1

Base Price: ₹ 30,074.34

GST (18%): ₹ 5,413.381

Total Price: ₹ 35,487.721

Certifications/Compliance

cGMP

Species

Horse

Quantity

500 mL

Endotoxin Concentration

≤5EU/ mL

Hemoglobin Concentration

<20 mg/dL

Osmolality

315 ± 35mOsm/kg

Protein Content

6 ± 2 g/dL

Content And Storage

-25° to -15°C

Product Type

Equine Serum

Sterility

Sterile

For Use With (Application)

Used in testing media for mycoplasma contamination or as a blocking agent and controls in immunoassays. It can also be combined with fetal bovine serum for the culture of rat adrenal pheochromocytoma (PC12) cells.

Mycoplasma Detected

No

pH

7.8 ± 0.8

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Description

  • Donor horse serum (DHS) is defined as the liquid fraction of clotted blood derived from horses from a closed, controlled standing herd that is under veterinary supervision and routinely monitored for various equine diseases
  • DHS can be used for various cell culture and immunochemical assays and is used to product antitoxins to a variety of diseases
  • Learn more about our custom serum options
  • Sera Processing Using industry leading techniques, blood is aseptically collected from a closed, controlled standing herd, serum is then isolated from the red blood cells and immediately frozen for testing and further processing
  • The raw sera is then true pooled and is 0.2 micron sterile filtered with a Sterility Assurance Level (SAL) of 10-3
  • Every lot then must pass USP <71> sterility testing and test negative for mycoplasma and number of industry-monitored viruses
  • Additional testing includes endotoxin, hemoglobin, pH, osmolality, total protein and a biochemical profile that contains various metals, proteins, hormones and other metabolites
  • ' Compliance Sera is aseptically collected and processed in a facility that is compliant with FDA guidelines for Class I Medical Devices.