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CRISPR Gene Editing : Methods and Protocols / edited by Yonglun Luo.

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Holman Biotech Commons QH506 .M45 v.1 (1984)-v.20 (1993),v.22 (1994),v.24 (1994)-v.53 (1996), v.42 (1995) and v.51 (1995) reported missing 3-13-2000 v.55 (1995),v.58 (1996)-v.63 (1997), v.65 (1996)-v.154 (2001), v.156 (2001)-190 (2002), v.192 (2002)-v.407 (2007) v.409 (2007)-v.416 (2008),v.418 (2008)-v.466 v.468-v.490,v.492,v.494,v.496-499 501-506,508,510-512,514,516-517,519-536 538,540-569,571 573-589,591-608,610-615,617,620-627,630-633,636,638,642
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Format:
Book
Contributor:
Luo, Yonglun, editor.
SpringerLink (Online service)
Series:
Springer Protocols (Springer-12345)
Methods in molecular biology 1064-3745 ; 1961.
Methods in Molecular Biology, 1064-3745 ; 1961
Language:
English
Subjects (All):
Human genetics.
Genetic engineering.
Human Genetics.
Genetic Engineering.
Local Subjects:
Human Genetics.
Genetic Engineering.
Physical Description:
1 online resource (XI, 362 pages) : 76 illustrations, 61 illustrations in color.
Edition:
First edition 2019.
Contained In:
Springer eBooks
Place of Publication:
New York, NY : Springer New York : Imprint: Humana, 2019.
System Details:
text file PDF
Summary:
This detailed volume guides readers through strategic planning and user-friendly guidelines in order to select the most suitable CRISPR-Cas system and target sites with high activity and specificity. Methods covering CRISPR gRNA design, CRISPR delivery, CRISPR activity quantification (indel quantification), and examples of applying CRISPR gene editing in human pluripotent stem cells, primary cells, gene therapy, and genetic screening are included. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and invaluable, CRISPR Gene Editing: Methods and Protocols will assist undergraduates, graduates, and researchers with detailed guidelines and methods for the vitally important CRISPR gene editing field. Chapter 3 is available open access under a CC BY 4.0 license via link.springer.com.
Contents:
CRISPR-gRNA Design
Tracking CRISPR's Footprints
Rapid Quantitative Evaluation of CRISPR Genome Editing by TIDE and TIDER
Fast and Quantitative Identification of Ex Vivo Precise Genome Targeting-Induced Indel Events by IDAA
Functional Evaluation of CRISPR Activity by the Dual-Fluorescent Surrogate System: C-Check
CRISPR-Cas9 Delivery by Artificial Virus (RRPHC)
Production and Validation of Lentiviral Vectors for CRISPR/Cas9 Delivery
Rapid and Simple Screening of CRISPR Guide RNAs (gRNAs) in Cultured Cells Using Adeno-Associated Viral (AAV) Vectors
Electroporation-Based CRISPR/Cas9 Gene Editing Using Cas9 Protein and Chemically Modified sgRNAs
Efficient Gene Editing of Human Induced Pluripotent Stem Cells Using CRISPR/Cas9
Editing the Genome of Human Induced Pluripotent Stem Cells Using CRISPR/Cas9 Ribonucleoprotein Complexes
Conditional Gene Knockout in Human Cells with Inducible CRISPR/Cas9
CRISPR/Cas9 as a Genome Editing Tool for Targeted Gene Integration in CHO Cells
Rapid and Efficient Gene Deletion by CRISPR/Cas9
Genome Editing in Mice
CRISPR/Cas9-Mediated Gene Tagging: A Step-by-Step Protocol
Gene Editing in Primary Cells of Cattle and Pig
Toward In Vivo Gene Therapy Using CRISPR
CRISPR Gene Therapy of the Eye: Targeted Knockout of Vegfa in Mouse Retina by Lentiviral Delivery
In Vivo Editing of the Adult Mouse Liver Using CRISPR/Cas9 and Hydrodynamic Tail Vein Injection
CRISPR-Based Lentiviral Knockout Libraries for Functional Genomic Screening and Identification of Phenotype-Related Genes.
Other Format:
Printed edition:
ISBN:
978-1-4939-9170-9
9781493991709
Access Restriction:
Restricted for use by site license.

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