SBI/Exosome-depleted FBS Media Supplement Heat Inactivated – USA Certified??????/EXO-FBSHI-250A-1/250 mL
基因編輯
商品編號
EXO-FBSHI-250A-1
品牌
SBI
公司
System Biosciences(SBI)
公司分類(lèi)
exosome isolation
商品信息
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Overview:
Avoid inadvertently studying bovine exosomes with heat inactivated Exo-FBS
Fetal bovine serum, or FBS, is an important component of many types of cell culture media, and some researchers require heat inactivated FBS. But for researchers interested in isolating exosomes from cultured cells, standard heat inactivated FBS can introduce unwanted complications—bovine exosomes, which can cause significant background issues or interfere with functional studies. Which is why
SBI
developed heat inactivated Exo-FBS, our patented exosome-depleted FBS.
Heat inactivated using a highly quality-controlled process
Exosome-sized vesicles removed
Very low levels of CD63-positive cow exosomes
Undetectable levels of cow miRNAs
Comparable growth rates as standard FBS
Interchangeable with standard FBS (add 10% in DMEM or RPMI)
Supporting Data:
High quality and great performance
Exo-FBS has greatly reduced levels of bovine exosomes (Figures 1 and 2), bovine miRNAs (Figure 3), and is even cleaner than ultracentrifuged FBS (Figure 4). Cell growth in media supplemented with Exo-FBS is similar to cell growth in media supplemented with standard FBS (Figure 5).
Exo-FBS has greatly reduced levels of bovine exosomes
Figure 1.
NanoSight particle analysis shows low levels of exosomes in Exo-FBS.
While standard FBS contains exosome-sized particles (top panels), Exo-FBS shows almost no particles (bottom panels). Standard FBS and Exo-FBS samples were diluted 1:1000 and then analyzed for particle size and abundance using a NanoSight LM10 instrument.
Figure 2. Bovine α
-CD63
ELISA
shows low levels of exosomes in Exo-FBS
CD63 is an exosome-specific
Marker
. An α-CD63
ELISA
of standard FBS and Exo-FBS shows very low levels of CD63 in Exo-FBS, supporting the NanoSight particle analysis which showed low numbers of exosome-sized particles in Exo-FBS (Figure 1). Equal volumes (50 ?l) of either standard FBS or Exo-FBS depleted media supplement were used and the graphed results normalized to the signal level of standard FBS.
Figure 3. qPCR assays show undetectable levels of bovine exosomal miRNAs in Exo-FBS.
While standard FBS contains amplifiable miRNAs (12 of the 72 individual miRNAs tested, left panels), Exo-FBS shows no amplifiable miRNAs (right panels). Standard FBS and Exo-FBS media supplements (4 ml) were treated with Trizol extraction methods to recover exosomal RNAs. RNA was converted to
CDN
A and 72 individual bovine microRNAs were measured by qPCR using
SBI
’s QuantiMir system.
Figure 4. NanoSight analysis shows Exo-FBS is cleaner than ultracentrifuged FBS.
Quality Control data is generated on every batch of Exo-FBS produced at
SBI
by comparing NanoSight particle count analyses to the source FBS, FBS ultracentrifuged for 18 hours, and Exo-FBS. All samples were diluted 1:100 and data collected in triplicate.
Figure 5. Cells grown in 10% Exo-FBS show comparable growth rates to 10% standard FBS.
HT1080 fibrosarcoma cells, PC-3 prostate cancer cells, MCF-7 breast cancer cells, and HEK293 cells were seeded at either 10,000 or 20,000 cells and then cultured under standard conditions at 37°C with 5% CO2 for 5 days.
Citations:
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Marker
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Mol. Ther.
. 2017 Mar 1; 25(3):679-693. PM ID: 28159509
Sun, L, et al. (2017) Exosomes derived from human umbilical cord mesenchymal stem cells protect against cisplatin-induced ovarian granulosa cell stress and apoptosis in vitro.
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Zhou, X, et al. (2017) Exosome production and its regulation of EGFR during wound healing in renal tubular cells.
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. 2017 Mar 29;:ajprenal.00078.2017. PM ID: 28356285
Josson, S, Gururajan, M & WKChung, L. (2017) miRNA Characterization from the Extracellular Vesicles.
bio-protocol
. ; 7(4). Link: bio-protocol
McNicholas, K & Michael, MZ. (2017) Immuno-characterization of Exosomes Using Nanoparticle Tracking Analysis.
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Thesis
. ;. Link: Thesis
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Huang, JH, et al. (2017) Systemic Admi
NIST
ration of Exosomes Released from Mesenchymal Stromal Cells Attenuates Apoptosis, Inflammation and Promotes Angiogenesis after Contusion Spinal Cord Injury in Rats.
J. Neurotrauma
. 2017 Jun 30;. PM ID: 28665182
Harischandra, DS, et al. (2017) Environmental neurotoxicant manganese regulates exosome-mediated extracellular miRNAs in cell culture model of Parkinson’s disease: Relevance to α-synuclein misfolding in metal neurotoxicity.
Neurotoxicology
. 2017 Apr 24;. PM ID: 28450057
Crookenden, MA, et al. (2017) Effect of circulating exosomes from transition cows on M
ADI
n-Darby bovine kidney cell function.
J. Dairy Sci.
. 2017 Jul 1; 100(7):5687-5700. PM ID: 28456398
Philley, JV, et al. (2017) Exosome secretome and mediated signaling in breast cancer patients with nontuberculous mycobacterial disease.
Oncotarget
. 2017 Mar 14; 8(11):18070-18081. PM ID: 28160560
Rashed, MH, et al. (2017) Exosomal miR-940 maintains SRC-mediated oncogenic activity in cancer cells: a poss
IBL
e role for exosomal disposal of tumor suppressor miRNAs.
Oncotarget
. 2017 Mar 21; 8(12):20145-20164. PM ID: 28423620
Huang, MB, et al. (2017) Secretion modification region-derived peptide blocks exosome release and mediates cell cycle arrest in breast cancer cells.
Oncotarget
. 2017 Feb 14; 8(7):11302-11315. PM ID: 28076321
Lambrecht, J, et al. (2017) Circulating ECV-Associated miRNAs as Potential Clinical Bio
Marker
s in Early Stage HBV and HCV Induced Liver Fibrosis.
Front Pharmacol
. 2017 Feb 24; 8:56. PM ID: 28232800
Xin, H, et al. (2017) Secondary Release of Exosomes From Astrocytes Contributes to the Increase in Neural Plasticity and Improvement of Functional Recovery After Stroke in Rats Treated With Exosomes Harvested From MicroRNA 133b-Overexpressing Multipotent Mesenchymal Stromal Cells.
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產(chǎn)品貨號:8210.4