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Basic Cell Culture Protocols

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Cover of 'Basic Cell Culture Protocols'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Detection of mycoplasma contaminations.
  3. Altmetric Badge
    Chapter 2 Eradication of mycoplasma contaminations.
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    Chapter 3 STR DNA Typing of Human Cell Lines: Detection of Intra- and Interspecies Cross-Contamination
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    Chapter 4 Classical and Molecular Cytogenetic Analysis
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    Chapter 5 Fluorescent In Situ Hybridization of DNA Probes in the Interphase and Metaphase Stages of the Cell Cycle
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    Chapter 6 The Development of T Lymphocytes in Fetal Thymus Organ Culture
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    Chapter 7 Generation, Isolation, and Engraftment of In Vitro-Derived Human T Cell Progenitors
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    Chapter 8 In Vitro Generation of Human T Regulatory Cells: Generation, Culture, and Analysis of FOXP3-Transduced T Cells.
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    Chapter 9 Simultaneous Cloning and Selection of Hybridomas and Transfected Cell Lines in Semisolid Media
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    Chapter 10 Isolation and characterization of mouse side population cells.
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    Chapter 11 Stem Cell Identification by DyeCycle Violet Side Population Analysis
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    Chapter 12 Isolation and Characterization of Cancer Stem Cells In Vitro
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    Chapter 13 Ex Vivo Differentiation of Cord Blood Stem Cells into Megakaryocytes and Platelets
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    Chapter 14 Generation and characterization of murine alternatively activated macrophages.
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    Chapter 15 Human Long-Term Culture Initiating Cell Assay
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    Chapter 16 Long-Term Culture-Initiating Cell Assay for Mouse Cells
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    Chapter 17 Colony Forming Cell Assays for Human Hematopoietic Progenitor Cells
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    Chapter 18 Studying Leukocyte Recruitment Under Flow Conditions
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    Chapter 19 Generation and Establishment of Murine Adherent Cell Lines
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    Chapter 20 Isolation, Enumeration, and Expansion of Human Mesenchymal Stem Cells in Culture
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    Chapter 21 Isolation and Culture of Mesenchymal Stem Cells from Mouse Compact Bone
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    Chapter 22 Generation of a Pool of Human Platelet Lysate and Efficient Use in Cell Culture
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    Chapter 23 In vitro methods to culture primary human breast epithelial cells.
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    Chapter 24 Human Prostate Epithelial Cell Cultures
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    Chapter 25 Enzymatic dissociation, flow cytometric analysis, and culture of normal mouse mammary tissue.
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    Chapter 26 Isolation and Characterization of Human Hair Follicle Epithelial Cells
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    Chapter 27 Cocultivation of Human Oral Keratinocytes and Human Osteoblast-Like Cells
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    Chapter 28 Isolation and Culture of Skeletal Muscle Myofibers as a Means to Analyze Satellite Cells
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    Chapter 29 Hepatic Differentiation of Embryonic Stem Cells by Murine Fetal Liver Mesenchymal Cells
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    Chapter 30 Methods to Culture, Differentiate, and Characterize Neural Stem Cells from the Adult and Embryonic Mouse Central Nervous System
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    Chapter 31 Feeder-Independent Culture Systems for Human Pluripotent Stem Cells
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    Chapter 32 Formation of Embryoid Bodies from Human Pluripotent Stem Cells Using AggreWell™ Plates
  34. Altmetric Badge
    Chapter 33 Techniques in Embryoid Body Formation from Human Pluripotent Stem Cells
Attention for Chapter 23: In vitro methods to culture primary human breast epithelial cells.
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Chapter title
In vitro methods to culture primary human breast epithelial cells.
Chapter number 23
Book title
Basic Cell Culture Protocols
Published in
Methods in molecular biology, November 2012
DOI 10.1007/978-1-62703-128-8_23
Pubmed ID
Book ISBNs
978-1-62703-127-1, 978-1-62703-128-8
Authors

Raouf A, Sun YJ, Afshin Raouf, Yu Jia Sun, Raouf, Afshin, Sun, Yu Jia

Abstract

Current evidence suggests that much like leukemia, breast tumors are maintained by a small subpopulation of tumor cells that have stem cell properties. These cancer stem cells are envisaged to be responsible for tumor formation and relapse. Therefore, knowledge about their nature will provide a platform to develop therapies to eliminate these breast cancer stem cells. This concept highlights the need to understand the mechanisms that regulate the normal functions of the breast stem cells and their immediate progeny as alterations to these same mechanisms can cause these primitive cells to act as cancer stem cells. The study of the primitive cell functions relies on the ability to isolate them from primary sources of breast tissue. This chapter describes processing of discarded tissue from reduction mammoplasty samples as sources of normal primary human breast epithelial cells and describes cell culture systems to grow single-cell suspensions prepared from these reduction samples in vitro.

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X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 29%
Other 3 18%
Student > Bachelor 2 12%
Professor 2 12%
Student > Ph. D. Student 1 6%
Other 2 12%
Unknown 2 12%
Readers by discipline Count As %
Medicine and Dentistry 6 35%
Agricultural and Biological Sciences 5 29%
Immunology and Microbiology 2 12%
Biochemistry, Genetics and Molecular Biology 1 6%
Engineering 1 6%
Other 0 0%
Unknown 2 12%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 31 January 2013.
All research outputs
#14,743,944
of 22,694,633 outputs
Outputs from Methods in molecular biology
#4,652
of 13,046 outputs
Outputs of similar age
#172,987
of 277,032 outputs
Outputs of similar age from Methods in molecular biology
#175
of 351 outputs
Altmetric has tracked 22,694,633 research outputs across all sources so far. This one is in the 32nd percentile – i.e., 32% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,046 research outputs from this source. They receive a mean Attention Score of 3.3. This one has gotten more attention than average, scoring higher than 59% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 277,032 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 35th percentile – i.e., 35% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 351 others from the same source and published within six weeks on either side of this one. This one is in the 48th percentile – i.e., 48% of its contemporaries scored the same or lower than it.