Complement, Guinea Pig Serum, is suitable for evaluating functional activity of human complement components and for other research requiring a high level of hemolytic activity.
Synonyme(s) :
Complement Serum, Guinea Pig Serum
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Complement, Guinea pig serum is suitable for evaluating the functional activity of human complement components and for other research requiring a high level of hemolytic activity.
Application
Complement, Guinea pig serum has been used:
as a component of M2 medium for differential staining of blastocysts[1]
along with anti-human whole serum antibody to remove trophectoderm (TE) by immunosurgery[2]
in influenza microneutralization assay and complement-dependent cytotoxicity (CDC) assay[3]
Actions biochimiques/physiologiques
Functionally equivalent to reference standard 71383
Avertissement
Toxicity: Standard Handling (A)
Reconstitution
Following reconstitution and sterile filtration, aliquot, and freeze (-70°C). Stock solutions are stable for up to 1 year at -70°C.
Reconstitute with 5 ml of sterile, distilled H₂O. It is recommended that the reconstituted material be filter sterilized.
Informations légales
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Iranian journal of reproductive medicine, 10(6), 555-560 (2012-11-01)
Indisputable population exposure to widespread electromagnetic fields, has grown concerns over the probable health effects of these fields. The present study was aimed to examine the possible effects of 50 Hz extremely low frequency electromagnetic field (ELF-EMF) exposure on the
For human embryonic stem cells (hESCs) to be used clinically, it is imperative that immune responses evoked by hESCs and their derivates after transplantation should be prevented. Human leukocyte antigens (HLA) and ABO blood group antigens are important histocompatibility factors
Journal of the Chemical Society. Perkin Transactions 1, 2979-2979 (1993)
Vaccines to generate durable humoral immunity against antigenically evolving pathogens such as the influenza virus must elicit antibodies that recognize conserved epitopes. Analysis of single memory B cells from immunized human donors has led us to characterize a previously unrecognized
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