Switch to film designated for chemiluminescent detection such as
BioMax® Light, MS, and MR.
Extraneous
spots
Aggregated protein or
antibody conjugate
Centrifuge the conjugate solution at 10,000
Negative
Control shows
PCR product
(signal)
Reagents or reactions
have been
contaminated
Extraneous DNA template may have been introduced into the
reagents or when setting up the PCR reactions.
Negative
Control shows
PCR product
(signal)
Reagents or reactions
have been
contaminated
Extraneous DNA template may have been introduced into the
reagents or when setting up the PCR reactions.
with a minimum of
vector-encoded extraneous amino acids.
NEW PRODUCTS
Vectors for expression of amino-terminal His•Tag® fusion proteins containing
minimal extraneous sequences
Eight new expression
new diagnostic tests requires the removal and
monitoring of contaminants, such as nucleases and
extraneous DNA, and creates new criteria for water purity
and water system design. Current water purification
and start the GC.
3. Run the GC program until completed.
4. There are typically some extraneous peaks in the
initial runs.
5. Repeat the step again to see
chromatography (IMAC) systems for His-tagged protein purification utilize a charged chelate linkage. Extraneous charges on the
resin will attract any oppositely charged amino acid in a protein, thereby increasing
each slide using a pencil only. A pen or
marker may affect the final results by introducing
extraneous background fluorescence.
2. Wash each slide briefly by dipping in PBS.
3. In a tube, mix
each slide using a pencil only. A pen or a
marker may affect the final results by introducing
extraneous background fluorescence.
2. Wash each slide briefly by dipping in PBS.
3. In a tube, mix 10–
each slide using a pencil only. A pen or a
marker may affect the final results by introducing
extraneous background fluorescence.
2. Wash each slide briefly by dipping in PBS.
3. In a tube, mix 50–
Coomassie Blue stained, 10% SDS-PAGE gel. Lack of protease activity is judged by
the presence of no extraneous bands on the gel.
Optimization of digestion for other proteins may involve: (1) Variation
Coomassie Blue stained, 10% SDS-PAGE gel. Lack of protease activity is judged by
the presence of no extraneous bands on the gel.
Optimization of digestion for other proteins may involve: (1) Variation
Coomassie Blue stained, 10% SDS-PAGE gel. Lack of protease activity is judged by
the presence of no extraneous bands on the gel.
Optimization of digestion for other proteins may involve: (1) Variation
allowing customers to see
at a glance the contents of the box or vial. We do not allow
extraneous design elements that might detract from a label’s
ability to convey important information about
high quality is the key
to the success of a MALDI-MS experiment. Organic
impurities can lead to extraneous peaks, especially in
the low mass range. Trace levels of ions, especially Na+
and K+, form adducts