BriClone SF Hybridoma Cloning Medium (BR-002)

Note: This product has a $35.00 Dry Ice Fee.
Host Quantity Applications Species Reactivity Data Sheet  
100 mL Cell Culture
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SKU: BR-002 Category: Tag:
Overview
Product Name BriClone SF Hybridoma Cloning Medium (BR-002)
Description BriClone SF is a Serum Free additive for the cloning medium used in the post-fusion stages of hybridoma production and for improving the efficiency of hybridoma cells cloning.
Applications Cell Culture
Properties
Form Liquid
Concentration 20X Solution
Background BriClone SF completely replaces the need for feeder cells. The use of feeder cells to support the outgrowth of hybridomas has many disadvantages, like batch-to-batch variation of the feeder cells and competition between feeder cells and freshly-fused hybridomas for nutrients in the culture medium. BriClone has been specially developed to overcome these common problems in the post-fusion period.
Specificity Information
Application Images
Description Percentage of fusion efficiency from freshly fused hybridomas cultured using BriClone (red) compared to Bri-Clone-SF (brown) and a negative control (blue).
Description BriClone-SF has equivalent fusion efficiency activity when compared to two leading competitor products when used at the manufacturer’s recommended concentrations. Percentage of fusion efficiency from freshly fused hybridomas cultured using BriClone-SF (orange) compared to Competitor A (light grey) and competitor B (dark grey) products and a negative control (blue).
Description BriClone-SF is stable for at least 9 months when stored at -20˚C. Percentage of fusion efficiency from freshly fused hybridomas cultured using BriClone-SF stored at 4˚C for 2 weeks, Room Temperature for 1 week and -20˚C for 9 months compared to a negative control (blue).
Additional Information
Additional Information BriClone is produced by exposing basal culture medium with a low percentage of foetal calf serum to a human cancer cell line, which secretes relevant molecules into the medium, resulting in a product consistently upportive of the fusion and cloning stages of hybridoma production. Some researchers require a product which is serum-free and has had no contact with human or animal cells. We have, therefore, designed BriClone-SF which has the same basal medium and biological activities as BriClone but has no added serum or other substances of human or animal origin and has not been exposed to cells. BriClone-SF contains added recombinant human proteins produced in bacterial or yeast host cells.

Quality Control
Each batch of BriClone-SF is tested for its ability to support / promote the growth of newly PEG fused hybridoma cells, plated in 48 well plates containing HAT selection medium with 5% BriClone-SF over a 10-12 day time period. Test cells used are Sp2/0-Ag14 mouse myeloma cells and immune splenocytes isolated from BALB/c mice.

-This product is for in vitro research purposes only. Not for human or veterinary use.
-Always use BriClone under aseptic conditions
-This product has been produced using cells that have not been screened for Hepatitis B, Human immunodeficiency viruses or other agents.
-Handle as a potentially biohazardous material under at least Biosafety Level 1 containment.
Handling
Storage Store at -20˚C. Avoid repeated freeze/thaw cycles. Stable for short periods at +4˚C
Dilution Instructions Thaw and add to the hybridoma cloning medium as a 5% v/v supplement.
Application Instructions Thaw and add to the hybridoma cloning medium as a 5% v/v supplement. BriClone SF can be used for:
• Hybridoma growth post-fusion (refer to your own protocol)
• Hybridoma Cloning (refer to your own protocol)
References & Data Sheet
References PMC7873262,PMC7239657,PMC6803335,PMC6816435,PMC6719973,PMC5017023,PMC2812581,PMC2896538,PMC4617144,PMC3944398,PMC9030397,PMC8470961,PMC8104110,PMC7279471,PMC7096428,PMC5992998,PMC5986985,PMC5857169,PMC4921032,PMC4591809,PMC4135088,PMC1858089,PMC1602225
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Establishment of monoclonal anti-human CD26 antibodies suitable for immunostaining of formalin-fixed tissue Ryo Hatano, Taketo Yamada, Shuji Matsuoka, Satoshi Iwata, Hiroto Yamazaki, Eriko Komiya, Toshihiro Okamoto, Nam H Dang, Kei Ohnuma, Chikao Morimoto Diagn Pathol. 2014; 9: 30. Published online 2014 Feb 6. doi: 10.1186/1746-1596-9-30

Development and Characterization of Anti-Naja ashei Three-Finger Toxins (3FTxs)-Specific Monoclonal Antibodies and Evaluation of Their In Vitro Inhibition Activity Ernest Z. Manson, Mutinda C. Kyama, Josephine Kimani, Aleksandra Bocian, Konrad K. Hus, Vladimír Petrilla, Jaroslav Legáth, James H. Kimotho Toxins (Basel) 2022 Apr; 14(4): 285. Published online 2022 Apr 16. doi: 10.3390/toxins14040285

Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism Natalie Young, Maria Asif, Matthew Jackson, Daniel Martín Fernández-Mayoralas, Mar Jimenez de la Peña, Beatriz Calleja-Pérez, Sara Álvarez, Eve Hunter-Featherstone, Angelika A. Noegel, Wolfgang Höhne, Peter Nürnberg, Boguslaw Obara, Muhammad Sajid Hussain, Iakowos Karakesisoglou, Alberto Fernández-Jaén Genes (Basel) 2021 Sep; 12(9): 1294. Published online 2021 Aug 24. doi: 10.3390/genes12091294

Antibody Screening System Using a Herpes Simplex Virus (HSV)-Based Probe To Identify a Novel Target for Receptor-Retargeted Oncolytic HSVs Hitomi Ikeda, Hiroaki Uchida, Yu Okubo, Tomoko Shibata, Yasuhiko Sasaki, Takuma Suzuki, Mika Hamada-Uematsu, Ryota Hamasaki, Kosaku Okuda, Miki Yamaguchi, Masaki Kojima, Masato Tanaka, Hirofumi Hamada, Hideaki Tahara J Virol. 2021 May; 95(9): e01766-20. Prepublished online 2021 Feb 24. Published online 2021 Apr 12. doi: 10.1128/JVI.01766-20

Isolation and Characterization of Antibodies Induced by Immunization with TNF-α Inducible Globotetraosylceramide Tetsuya Okuda Int J Mol Sci. 2020 May; 21(10): 3632. Published online 2020 May 21. doi: 10.3390/ijms21103632

CDK1 dependent phosphorylation of hTERT contributes to cancer progression Mami Yasukawa, Yoshinari Ando, Taro Yamashita, Yoko Matsuda, Shisako Shoji, Masaki Suimye Morioka, Hideya Kawaji, Kumiko Shiozawa, Mitsuhiro Machitani, Takaya Abe, Shinji Yamada, Mika K. Kaneko, Yukinari Kato, Yasuhide Furuta, Tadashi Kondo, Mikako Shirouzu, Yoshihide Hayashizaki, Shuichi Kaneko, Kenkichi Masutomi Nat Commun. 2020; 11: 1557. Published online 2020 Mar 25. doi: 10.1038/s41467-020-15289-7

Data on immunoglobulin G antibodies induced by immunization of mice with globoside carrying very long-chain fatty acids Tetsuya Okuda Data Brief. 2018 Aug; 19: 256–260. Published online 2018 May 10. doi: 10.1016/j.dib.2018.05.014

Detection of high CD44 expression in oral cancers using the novel monoclonal antibody, C44Mab-5 Shinji Yamada, Shunsuke Itai, Takuro Nakamura, Miyuki Yanaka, Mika K. Kaneko, Yukinari Kato Biochem Biophys Rep. 2018 Jul; 14: 64–68. Published online 2018 Apr 12. doi: 10.1016/j.bbrep.2018.03.007

Detection of high PD-L1 expression in oral cancers by a novel monoclonal antibody L1Mab-4 Shinji Yamada, Shunsuke Itai, Mika K. Kaneko, Yukinari Kato Biochem Biophys Rep. 2018 Mar; 13: 123–128. Published online 2018 Feb 6. doi: 10.1016/j.bbrep.2018.01.009

Establishment of anti-mesothelioma monoclonal antibodies Natsuko Mizutani, Masaaki Abe, Shuji Matsuoka, Kazunori Kajino, Midori Wakiya, Naomi Ohtsuji, Ryo Hatano, Chikao Morimoto, Okio Hino BMC Res Notes. 2016; 9: 324. Published online 2016 Jun 24. doi: 10.1186/s13104-016-2128-x

Cellular Interaction and Cytotoxicity of the Iowa Mutation of Apolipoprotein A-I (ApoA-IIowa) Amyloid Mediated by Sulfate Moieties of Heparan Sulfate Kaori Kuwabara, Kazuchika Nishitsuji, Kenji Uchimura, Shang-Cheng Hung, Makoto Mizuguchi, Hiroyuki Nakajima, Shiho Mikawa, Norihiro Kobayashi, Hiroyuki Saito, Naomi Sakashita J Biol Chem. 2015 Oct 2; 290(40): 24210–24221. Published online 2015 Aug 19. doi: 10.1074/jbc.M115.652545

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