CultureBoost™ Growth Factor (2x5mL)
CultureBoost™ Growth Factor (2x5mL)
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- PRODUCT INFO
- USE CASES
Gain Consistency with our Single Lot Media and Reagents
CultureBoost™ is the broad-spectrum mitogen in Cell Systems Complete Medium (4Z0-500) and Cell Systems Medium Without Serum (4Z3-500). CultureBoost contains Cell Systems bovine growth factor and porcine heparin. One 5mL vial of CultureBoost™ supplements one 500mL bottle of media.
CultureBoost™ is purified from bovine pituitary or hypothalamus and is 100% traceable to cattle processed in the USA at USDA inspected facilities. The product's working concentration is 50µg/mL. Biological activity is adjusted to 110% of maximum using CSC 2V0 Human Venous Endothelial cells, ACBRI 181 Primary Retinal Microvascular Endothelial cells, and ACBRI 376 Primary Brain Microvascular Endothelial cells.
CultureBoost™ is qualified for use with Cell Systems media, and when initiating, thawing, expanding or passaging cultures of all mesenchymal-derived cells.
Use of CultureBoost™ can result in as much as 25% increase in recovery from freezing, an increase of 10-20% in cell count per passage, and a one day decrease in time-to-confluence. The effects of CultureBoost™ are most pronounced with extremely fastidious cells.
A 5mL vial is included in various Cell Systems media kits and in "The System™". CultureBoost™ 2x5mL vials are also available individually here.
Storage and Handling
This product is delivered at ambient temperature. Use 10ml to supplement 500ml cell culture medium. If the entire unit will not be used within 30 days, aliquot and freeze. Once opened, shelf life is 30 days at +2-8°C.
Cell Systems media and reagents are made with WFI, all components are cGMP and ISO Compliant, and are classified "Sterile".
A Selection of Citations for 4CB-500 from Scientific Journals
Discover additional research on Google Scholar that utilizes Cell Systems CultureBoost™.
"Improvement in diabetic retinopathy through protection against retinal apoptosis in spontaneously diabetic Torii rats mediated by ethanol extract of Osteomeles schwerinae C.K. Schneid" Kim, Kim, Kim, et al. Nutrients, 2019.
- "SiRNA silencing of VEGF, IGFs, and their receptors in human retinal microvascular endothelial cells" Nicolau et al American J Translational Research, 2018
- "Human retinal endothelial cells and astrocytes cultured on 3-D scaffolds for ocular drug discovery and development" Beharry et al. Prostaglandins and Other Lipid Mediators, 2018
"Tangential flow filtration for highly efficient concentration of extracellular vesicles from large volumes of fluid" Busatto and Vilanilam et al. Cells, 2018.
"Barrier properties and transcriptome expression in human iPSC‐derived models of the blood–brain barrier" Delsing et al. Stem Cells, 2018.
- "MnTBAP or catalase Is more protective against oxidative stress in human retinal endothelial cells exposed to Intermittent hypoxia than their co-administration" Quan et al. Reactive Oxygen Species, 2017
"Association of HMGB1 with oxidative stress markers and regulators in PDR" Abu El-Asrar and Alam et al. Molecular Vision, 2017.
"Neuropilin-1 modulates interferon-γ-stimulated signaling in brain microvascular endothelial cells" Wang et al. Journal of Cell Science, 2016.
"Fenofibrate Inhibits cytochrome P450 epoxygenase 2C activity to suppress pathological ocular angiogenesis" Gong et al. EBioMedicine, 2016.
"Primary human liver co-culture With flow and Kupffer cell integration on microfluidic liver-on-a-chip" Mazur (Dissertation thesis), 2015.
"Aflibercept traps galectin-1, an angiogenic factor associated with diabetic retinopathy" Kanda et al. Scientific Reports, 2015.
"Chemokine receptor CXCR7 is a functional receptor for CXCL12 in brain endothelial cells" Liu et al. PLoS One, 2014.
"S100A4 is upregulated in proliferative diabetic retinopathy and correlates with markers of angiogenesis and fibrogenesis" Abu El-Asrar et al. Molecular Vision, 2014.
"Differential expression and role of hyperglycemia induced oxidative stress in epigenetic regulation of β1, β2 and β3-adrenergic receptors in retinal endothelial cells" Safi et al. BMC Medical Genomics, 2014.
"Optical recording reveals novel properties of GSK1016790A-induced vanilloid transient receptor potential channel TRPV4 activity in primary human endothelial cells" Sullivan et al. Molecular Pharmacology, 2012.
"High-glucose-induced endothelial cell injury is inhibited by a peptide derived from human Apolipoprotein E" Bhattacharjee et al. PLoS One, 2012.
CultureBoost™ has two main uses.
1. Application as a growth supplement to medium:
CultureBoost™ can be purchased separately (4CB-500) to supplement Cell Systems Media Kit without Growth Factor (4Z0-500-S) or other cell culture media.
2. Application in the vial thaw procedure:
Cells are at their most fragile when in recovery from thawing or passage. The growth factors in CultureBoost™ and CultureBoost-R™ stabilize the plasma membrane and provide a concentrated dose of factors that have been shown to aid the cell in attachment, activation, and achievement of polarity.
CultureBoost™ can be beneficially used any time cells are "loosened" from the pellet prior to resuspension in Cell Systems Medium in preparation for plating. The best results of using CultureBoost™ are evident when 50-100 microliters are added to the loosened cell pellet just prior to re-suspension in medium. Please refer to the instructions for our Passage Reagent Group™ (4Z0-800).