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12449C

Sigma-Aldrich

Horse Serum

USA origin, Donor herd, suitable for cell culture, suitable for hybridoma

Synonym(s):

HS, equine sera, equine serum, horse sera, sera, serum

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About This Item

MDL number:
MFCD00164115
UNSPSC Code:
12352207
NACRES:
NA.71

biological source

horse serum

Quality Level

500

sterility

sterile-filtered

composition

hemoglobin, ≤20 mg/dL

origin

USA origin

technique(s)

cell culture | hybridoma: suitable
cell culture | mammalian: suitable

impurities

≤10 EU/mL endotoxin

shipped in

dry ice

storage temp.

−20°C

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Application

Donor Herd Serum is suitable for use in diagnostic assays, as a supplement in mycoplasma growth and assay media and for culturing hematopoietic stem and neuronal cells.

Other Notes

Donor Horse Serum is collected from controlled donor herds located in the USA. Horse serum contains high protein and low trace metals compared to Fetal Bovine Serum.

Preparation Note

Collected from a controlled herd.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Gemma Molyneux et al.
Toxicologic pathology, 37(2), 170-174 (2009-04-01)
In vitro techniques for the culture of hemopoietic stem cells and committed hemopoietic progenitor cells in rat bone marrow have not been adequately described in the literature. In the present investigations, and using commercially available hemopoietic cytokines and growth factors
Z C Ye et al.
Glia, 22(3), 237-248 (1998-03-03)
Serum is used widely for culturing neurons and glial cells, and is thought to provide essential, albeit undefined, factors such as hormones, growth factors, and trace elements that promote the growth of cells in vitro. Moreover, serum can have profound
Evangelos Delivopoulos et al.
Biomaterials, 30(11), 2048-2058 (2009-01-14)
This paper describes a simple technique for the patterning of glia and neurons. The integration of neuronal patterning to Multi-Electrode Arrays (MEAs), planar patch clamp and silicon based 'lab on a chip' technologies necessitates the development of a microfabrication-compatible method
Chandra Somasundaram et al.
Journal of vascular research, 43(3), 278-288 (2006-04-26)
Confocal analysis of the whole-mount rat mesenteric branch arteries (MBA) revealed nucleated structures with axonal processes which immunostained for calcitonin gene-related peptide (CGRP). Immunocytochemistry ruled out the possibility that these were immune elements (macrophages and mast or dendritic cells) in
Juulia H Lautaoja et al.
Biomolecules, 10(5) (2020-05-06)
Alongside in vivo models, a simpler and more mechanistic approach is required to study the effects of myostatin on skeletal muscle because myostatin is an important negative regulator of muscle size. In this study, myostatin was administered to murine (C2C12)
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