BIOAMF-1 Medium

Designed for the primary culture of human amniotic fluid cells and chorionic villi (CV) samples
nameSKUsize
BIOAMF™-1 Medium (US only)01-190-1A-KT500 mL
BIOAMF™-1 Medium (US only)01-190-1B-KT100 mL
BIOAMF™-1 Medium01-190-1A450 mL
BIOAMF™-1 Medium01-190-1B90 mL
BIOAMF™-1 Supplement01-192-1E50 mL
BIOAMF™-1 Supplement01-192-1D10 mL
  • Description
  • Specifications
  • References
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Description

BIOAMF-1 Medium Overview:

BIOAMF-1 medium is designed for the primary culture of human amniotic fluid cells and chorionic villi (CV) samples in both open (5% CO2) and closed systems. The medium allows rapid growth of amniocytes or chorionic villi for use in karyotyping.

No supplementation with serum or serum-substitutes is necessary. This medium consists of two components: basal medium and frozen supplement.

Storage and Stability

  • BIOAMF-1 Basal Medium is stable for 15 months from production date when stored at 2-8ºC.
  • BIOAMF-1 Supplement is stable for 24 months from production date when stored at -20ºC.
  • The complete medium is stable for 14 days when stored at 2-8ºC. Do not freeze the complete medium.
  • Protect both the basal medium and the complete medium from light.

Additional information

Brand

Shipping Conditions

Cold Pack

Storage Conditions

4ºC

  1. D. Schmidt, A. Mol, C. Breymann, J. Achermann, et l., Engineered From Human Prenatally Harvested Progenitors. Circulation 114: I-125 – I-131 (2006).
  2. Ç. Biray Avci, Z. Özlem Doğan, N. Oktar, et al., The Effect of Cyclosporin A Via P53, MDM2 and PIK3CA Gene Expressions in Glioblastoma Multiforme Cells. Journal of Neurological Sciences (Turkish) 27 (2): 170-177 (2010).
  3. D. Diego-Alvarez, C. Ramos-Corrales, M Garcia-Hoyos, et al., Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach. Human Reproduction 21(4): 958-966
  4. D. Diego-Alvarez , M. Rodriguez de Alba , R. Cardero-Merlo, et al., MLPA as a screening method of aneuploidy and unbalanced chromosomal rearrangements in spontaneous miscarriages. Prenatal Diagnosis 27(8): 765 – 771 (2007).
  5. N. Gregersen, V. Winter, P.K.A. Jensen, et al.,  Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhood. Prenatal Diagnosis 15 (1): 82 - 86 (2005).
  6. I. Vogel, T. Lyngbye , A. Nielsen , et al.,  Pallister-Killian syndrome in a girl with mild developmental delay and mosaicism for hexasomy 12p. American Journal of Medical Genetics Part A. 149A (3): 510 - 514 (2009).

Materials Safety Data Sheet

Manuals and Protocols

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