Fluorescence microscopy--avoiding the pitfalls.

نویسنده

  • Claire M Brown
چکیده

There was an error published in J. Cell Sci. 120, 1703-1705. On p. 1704, in the section ‘Image acquisition’, line 6 should read ‘all four pixels in a 2 2 square are summed into a single pixel’. For clarification, 2 2 binned pixels are twice the height and twice the width of the original pixel, but the pixel area is four times larger; similarly, for a 4 4 binned image the pixel height and width are four times larger, resulting in a pixel that has 16 times the area of the original pixels.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ultrastructural Diagnosis of Soft Tissue Tumors: Avoiding Pitfalls

The use of immunohistochemistry and, more recently, molecular methods has seen a sharp reduction of the role of electron microscopy in the diagnosis of soft tissue sarcomas (1,2). Ultrastructural analysis, however, does continue to play a useful role in selected cases. The focus in this presentation is on adult soft tissue tumors; Dr. John Hicks will follow with a presentation on avoiding pitfa...

متن کامل

A Thin Layer Imaging with the Total Internal Reflection Fluorescence Microscopy

Total internal reflection fluorescence microscopy (TIRFM) is an optical technique that allows imaging of a thin layer of the sample with a thickness of about 100-200 nm. It is used in science of cell biology to study cellular processes, especially near the membranes of living cells. This method is based on the total internal reflection phenomenon, where the evanescent wave is generated in the l...

متن کامل

Avoiding the pitfalls of single particle cryo-electron microscopy: Einstein from noise.

Single particle cryo-electron microscopy is currently poised to produce high-resolution structures of many biological assemblies, but several pitfalls can trap the unwary. This critique highlights one problem that is particularly relevant when smaller structures are being studied. It is known as "Einstein from noise," in which the experimenter honestly believes they have recorded images of thei...

متن کامل

Studying the Stoichiometry of Epidermal Growth Factor Receptor in Intact Cells using Correlative Microscopy.

This protocol describes the labeling of epidermal growth factor receptor (EGFR) on COS7 fibroblast cells, and subsequent correlative fluorescence microscopy and environmental scanning electron microscopy (ESEM) of whole cells in hydrated state. Fluorescent quantum dots (QDs) were coupled to EGFR via a two-step labeling protocol, providing an efficient and specific protein labeling, while avoidi...

متن کامل

Imaging cellular structures in super-resolution with SIM, STED and Localisation Microscopy: A practical comparison

Many biological questions require fluorescence microscopy with a resolution beyond the diffraction limit of light. Super-resolution methods such as Structured Illumination Microscopy (SIM), STimulated Emission Depletion (STED) microscopy and Single Molecule Localisation Microscopy (SMLM) enable an increase in image resolution beyond the classical diffraction-limit. Here, we compare the individu...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Journal of cell science

دوره 120 Pt 10  شماره 

صفحات  -

تاریخ انتشار 2007