13.03.2013 Views

2012 Promega catalogue

2012 Promega catalogue

2012 Promega catalogue

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Life<br />

Science<br />

Catalog<br />

<strong>2012</strong><br />

Worldwide Contact List<br />

Section<br />

Contents<br />

Table of<br />

Contents<br />

Cell Signaling<br />

238<br />

Transcend Non-Radioactive Translation<br />

Detection Systems<br />

Product Size Cat.# Price ($)<br />

Transcend Colorimetric Translation<br />

Detection System<br />

Transcend Chemiluminescent Translation<br />

30 reactions L5070 377.00<br />

Detection System<br />

Available Separately<br />

30 reactions L5080 566.00<br />

Transcend tRNA 30 µl L5061 307.00<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

Description: The Transcend Non-Radioactive Translation Detection<br />

Systems allow non-radioactive detection of proteins synthesized in vitro.<br />

Using these systems, biotinylated lysine residues are incorporated into<br />

nascent proteins during translation, eliminating the need for labeling with [ 35 S]<br />

methionine or other radioactive amino acids. This biotinylated lysine is added<br />

to the translation reaction as a precharged ε-labeled biotinylated lysine-tRNA<br />

complex (Transcend tRNA) rather than a free amino acid. After SDS-PAGE<br />

and electroblotting, the biotinylated proteins can be visualized by binding either<br />

Streptavidin-Alkaline Phosphatase (Streptavidin-AP) or Streptavidin-Horseradish<br />

Peroxidase (Streptavidin-HRP), followed either by colorimetric or chemiluminescent<br />

detection. Typically, these methods can detect 0.5–5ng of protein<br />

within 3–4 hours after gel electrophoresis. This sensitivity is equivalent to that<br />

achieved with [ 35 S]methionine incorporation and autoradiographic detection<br />

6–12 hours after gel electrophoresis.<br />

Features:<br />

• Sensitive: The biotin tag allows detection of 0.5–5ng of translated protein.<br />

• Safe: No radioisotope handling, storage or disposal is required.<br />

• Fast: Labeled proteins can be detected 3–4 hours after gel electrophoresis.<br />

• Flexible: Results can be visualized by using colorimetric or chemiluminescent<br />

detection.<br />

Storage Conditions: Store Transcend tRNA at –70°C. Do not subject<br />

the Transcend tRNA to more than five freeze-thaw cycles. Store all other<br />

components at 4°C.<br />

Protocol Part#<br />

Transcend Non-Radioactive Translation Detection System<br />

Technical Bulletin<br />

TB182<br />

ECL Western Blotting Substrate<br />

Product Size Cat.# Price ($)<br />

ECL Western Blotting Substrate 250 ml W1001 247.00<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

500 ml W1015 387.00<br />

Description: The ECL Western Blotting Substrate is a highly sensitive<br />

non-radioactive, enhanced luminol-based chemiluminescent substrate for the<br />

detection of horseradish peroxidase (HRP) on immunoblots. The ECL Western<br />

Blotting Substrate detects picogram amounts of antigen, and with the use of<br />

photographic or other imaging methods, visualizes the presence of HRP.<br />

Features:<br />

• High Sensitivity: Detect picogram levels of protein.<br />

• Save Time: No optimization required; you can switch from other entrylevel<br />

ECL substrates.<br />

Storage Conditions: Store at 2–8°C.<br />

Protocol Part#<br />

ECL Western Blotting Substrate Technical Manual TM317<br />

TMB One Solution<br />

Product Size Cat.# Price ($)<br />

TMB One Solution<br />

For Laboratory Use.<br />

100 ml G7431 144.00<br />

For additional information see page 176.<br />

AttoPhos ® AP Fluorescent Substrate System<br />

Product Size Cat.# Price ($)<br />

AttoPhos ® AP Fluorescent Substrate System<br />

AttoPhos<br />

3 × 36 mg S1000 727.00<br />

® AP Fluorescent Substrate System<br />

Trial Size<br />

Available Separately<br />

1 × 36 mg S1001 295.00<br />

AttoPhos ® Substrate 36 mg S1011 192.00<br />

100 mg S1012 474.00<br />

1 g S1013 1884.00<br />

AttoPhos ® Buffer 60 ml S1021 114.00<br />

240 ml S1022 349.00<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

Description: AttoPhos ® AP Fluorescent Substrate System contains a highly<br />

sensitive fluorescent alkaline phosphatase (AP) substrate.<br />

Features:<br />

• Sensitivity: Low fluorescence signal until enzymatically acted upon, yielding<br />

detection of AP to 0.1 attomole.<br />

• Low Background: Low fluorescence from interfering biological molecules.<br />

• Linearity: Linear kinetics over five orders of magnitude of AP concentration.<br />

• Additional Features: Excitation at 435nm, emission at 555nm and large<br />

Stokes’ shift (≈120nm).<br />

Storage Conditions: Store at 4°C.<br />

Protocol Part#<br />

AttoPhos ® AP Fluorescent Substrate System Technical Bulletin TB280<br />

Blocking Agents<br />

Product Size Cat.# Price ($)<br />

Blot-Qualified BSA 10 g W3841 87.00<br />

Tween ® 20<br />

For Laboratory Use.<br />

2.5 ml W3831 53.00<br />

Description: This BSA (bovine serum albumin) has been tested and qualified<br />

for optimum performance in immunoblotting applications with alkaline phosphatase<br />

antibody conjugates. It is shown to be alkaline phosphatase-free.<br />

Tween ® 20 is a nonionic detergent used as a buffer component for immunoscreening<br />

in the ProtoBlot ® Systems. In addition to blocking agents<br />

such as BSA, which saturate excess sites of antibody binding on membranes,<br />

this detergent acts in solution to dissociate nonspecific interactions with an<br />

antibody probe.<br />

For complete and up-to-date product information visit: www.promega.com/catalog

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!