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Principaux documents

N4762

Sigma-Aldrich

Newborn Calf Serum

USA origin, Heat Inactivated, sterile-filtered, suitable for cell culture

Synonyme(s) :

NBCS, NBS, NCS, calf sera, calf serum, newborn calf sera

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About This Item

Numéro MDL:
Code UNSPSC :
12352207
Nomenclature NACRES :
NA.71
Source biologique:
bovine (calf)
Origine:
USA origin
Stérilité:
sterile-filtered
Forme:
liquid
Conditions d'expédition:
dry ice
Le tarif et la disponibilité ne sont pas disponibles actuellement.

Source biologique

bovine (calf)

Niveau de qualité

Stérilité

sterile-filtered

Forme

liquid

Composition

hemoglobin, ≤20 mg/mL

Origine

USA origin

Technique(s)

cell culture | mammalian: suitable

Impuretés

≤100 EU/mL endotoxin

Conditions d'expédition

dry ice

Température de stockage

−20°C

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Application

NCS is useful in a wide range of cell culture and organ preservation applications. For example, it is used in cornea preservation and cryopreservation of bovine embryos. NCS is used in cell culture to support the maturation of oocytes; to study the function of tubular epithelial cells; and to develop primary cultures of cells such as visceral adipocytes.

Notes préparatoires

Collected from calves that are 10 days old or less.
Prepared by heating at 56°C for 30 minutes.

Remarque sur l'analyse

Endotoxin tested

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves


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Consulter la Bibliothèque de documents

Ümüt Cirit et al.
Theriogenology, 128, 218-224 (2019-02-21)
The present study evaluated follicular superstimulatory (FSS) and superovulatory (SOV) responses and in vivo embryo production in lactating Simmental cows treated with FSH starting 1 or 2 days after follicle aspiration (FA). The performance of a lengthened superovulation program, named 6dFSH-P36-hCG60
Mette Hemmingsen et al.
PloS one, 8(5), e63638-e63638 (2013-06-01)
High cell density is known to enhance adipogenic differentiation of mesenchymal stem cells, suggesting secretion of signaling factors or cell-contact-mediated signaling. By employing microfluidic biochip technology, we have been able to separate these two processes and study the secretion pathways.
Adela Ngwewondo et al.
Experimental parasitology, 198, 71-78 (2019-02-17)
Despite the efforts employed for the control of onchocerciasis, the latter has remained a significant public health problem, due mainly to the lack of safe and effective adult worm drugs and/or microfilaricides that do not kill Loa loa microfilariae (mf).
Ling Chen et al.
American journal of nephrology, 25(5), 459-465 (2005-08-25)
Oxidative stress has been considered to be a common pathogenetic factor of diabetic nephropathy. But the reason why renal cells are susceptible to oxidative injury in diabetes is not clear. Vitamin C plays a central role in the antioxidant defense
Kyoko Shimizu et al.
Cell biology international, 30(4), 381-388 (2006-03-15)
We have recently developed a primary culture system for visceral adipocytes (VAs) using stomal-vascular cells (SVCs) isolated from the mesenteric fat tissue of male Sprague-Dawley rats of 3-5 weeks of age. Modified Dulbecco's modified Eagle medium (DMEM)/F12 containing 17 microM

Articles

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Find answers to frequently asked questions (FAQs) about FBS and other serum products, and links to related products.

Questions

1–2 of 2 Questions  
  1. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  2. Why is serum Heat-Inactivated (HI)?

    1 answer
    1. Heat inactivation of serum is performed to inactivate complement (which can cause cell lysis or downstream problems in immunoassays). If there are immunoglobulins present in the serum that can bind to the cells in culture (either specifically or non-specifically), there is a chance for antibody-mediated complement cytotoxicity (ADCC, causing cell death). It may also reduce the titer of some mycoplasma and some viruses. Often, heat-inactivated serum is used because of the adoption of a previous protocol. It is mainly used when culturing hematopoetic cells or performing immunological type assays such as mixed-lymphocyte reactions or neutralization assays.FBS may not be heat inactivated as this is not required for all applications. It limits the loss of the other protein activity that may be minimally present in the serum.A protocol for heat inactivation:1. Allow serum containers to come to room temperature. Swirl bottles of serum immediately before adding to the water bath.2. A water-filled control bottles (T1) should be placed in a 56 °C water bath. Place the containers in the water bath up to the serum line. Do not completely submerge the containers. When the temperature of T1 reaches 56 °C, start the timer set for 30 minutes. Do not allow temperatures to exceed 56 °C. Higher temperatures will denature the proteins, gel the serum or alter the performance of the serum.3. Gently swirl the bottles every 5 to 10 minutes while in the water bath and check the temperature in the control bottle. It is not uncommon for plastic containers to bow slightly after heat treatment. This is not harmful to the serum.4. At the end of 30 minutes remove the serum bottles from the water bath. Aliquot the serum into smaller volumes and freeze. Sigma-Aldrich does not recommend repeated thaw-freeze cycles.

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