Correlative light and electron microscopy IV / edited by Thomas Müller-Reichert, Paul Verkade.

Contributor(s):

Material type: Text

TextSeries: Methods in cell biology ; v. 162.Publisher: Cambridge, MA : Academic Press, 2021Description: 1 online resourceContent type:

text

Media type:

computer

Carrier type:

online resource

ISBN:

9780128220597
0128220597

Subject(s): Genre/Form:

Additional physical formats: Print version:: No title; Print version:: No titleDDC classification:

570.2823 23

LOC classification:

QH212.E4 C67 2021

Online resources:

Click here to access online

Summary: Abstract: Correlative light and electron microscopy (CLEM) combines the strengths of light microscopy (LM) and electron microscopy (EM) to pin-point and visualize cellular or macromolecular structures. However, there are many different imaging modalities that can be combined in a CLEM workflow, creating a vast number of combinations that can overwhelm new-comers to the field. Here, we offer a conceptual framework to help guide the decision-making process for choosing the CLEM workflow that can best address your research question, based on the answer to five questions.

Holdings ( 1 )
Title notes ( 2 )

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Item type	Current library	Collection	Call number	Status	Date due	Barcode	Item holds
eBook	e-Library	eBook Elsevier		Available

Total holds: 0

Online resource; title from PDF title page (viewed August 16, 2021).

Abstract: Correlative light and electron microscopy (CLEM) combines the strengths of light microscopy (LM) and electron microscopy (EM) to pin-point and visualize cellular or macromolecular structures. However, there are many different imaging modalities that can be combined in a CLEM workflow, creating a vast number of combinations that can overwhelm new-comers to the field. Here, we offer a conceptual framework to help guide the decision-making process for choosing the CLEM workflow that can best address your research question, based on the answer to five questions.