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Product listing: Anti-rabbit IgG (H+L) (DyLight™ 680 Conjugate) #5366 to Tris-Glycine SDS Running Buffer (10X) #4050

$80
100 µl
$162
500 µl
Anti-rabbit IgG (H+L) was conjugated to DyLight™ 680 fluorescent dye under optimal conditions and formulated at 1 mg/ml. Excitation is 684 nm and peak fluorescence emission is 715 nm.

Background: Near infrared anti-species IgG conjugates are ideal for fluorescent western blotting and In-Cell Western. Cell Signaling Technology's strict quality control procedures assure that each conjugate provides optimal specificity and fluorescence.

$80
100 µl
$162
500 µl
Anti-rabbit IgG (H+L) was conjugated to DyLight™ 800 4X PEG fluorescent dye under optimal conditions and formulated at 1 mg/ml. Excitation is 777 nm and peak fluorescence emission is 794 nm.

Background: Near infrared anti-species IgG conjugates are ideal for fluorescent western blotting and In-Cell Western. Cell Signaling Technology's strict quality control procedures assure that each conjugate provides optimal specificity and fluorescence.

$142
1 ml
Affinity purified goat anti-rabbit IgG (H+L) antibody is conjugated to biotin. This product has been optimized for use as a secondary antibody in western blotting applications.
APPLICATIONS

Application Methods: Western Blotting

$142
250 µl
Anti-Rabbit IgG (H+L) F(ab')2 Fragment was conjugated to Alexa Fluor® 488 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F(ab')2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fc receptors.
APPLICATIONS

Application Methods: Flow Cytometry, Immunofluorescence (Immunocytochemistry)

$142
250 µl
Anti-Rabbit IgG (H+L) F(ab')2 Fragment was conjugated to Alexa Fluor® 555 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F(ab')2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fc receptors.
APPLICATIONS

Application Methods: Immunofluorescence (Immunocytochemistry)

$142
250 µl
Anti-rabbit IgG (H+L), F(ab')2 Fragment was conjugated to Alexa Fluor® 594 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F(ab')2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fc receptors.
APPLICATIONS

Application Methods: Flow Cytometry, Immunofluorescence (Immunocytochemistry)

$142
250 µl
Anti-rabbit IgG (H+L) F(ab')2 Fragment was conjugated to Alexa Fluor® 647 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This F(ab')2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fc receptors.
APPLICATIONS

Application Methods: Flow Cytometry, Immunofluorescence (Immunocytochemistry)

$199
250 µl
Anti-rabbit IgG (H+L), F(ab')2 Fragment was conjugated to phycoerythrin (PE) under optimal conditions. This F(ab')2 fragment product results in less non-specific binding, as it lacks the Fc domain that can bind to the cells with Fc receptors.
APPLICATIONS

Application Methods: Flow Cytometry

$203
250 µl
Anti-rabbit IgG (H+L), F(ab')2 Fragment was conjugated to phycoerythrin (PE) under optimal conditions and formulated at 1 mg/ml. This F(ab')2 fragment results in less non-specific binding to cells through Fc receptors.
APPLICATIONS

Application Methods: Flow Cytometry

$131
1 ml
This Cell Signaling Technology antibody is immobilized via covalent binding of primary amino groups to N-hydroxysuccinimide (NHS)-activated Sepharose® beads. Anti-rabbit IgG F(ab') 2 Fragment (Sepharose® Bead Conjugate) is useful for the immunoprecipitation of antibodies raised in rabbit.
APPLICATIONS

Application Methods: Immunoprecipitation

$142
1 ml
Affinity purified goat anti-rabbit IgG (H&L) antibody is conjugated to calf intestinal alkaline phosphatase. This product has been optimized for use as a secondary antibody in western blotting and ELISA applications.
APPLICATIONS

Application Methods: ELISA, Western Blotting

Background: The alkaline phosphatase (AP) conjugated secondary antibodies are utilized in conjunction with specific chemiluminescent or other substrates for detection on western blots. One of the advantages of AP conjugation is that the reaction rate remains linear for a long period of time.

$76
100 µl
$142
1 ml
$452
5 ml
Designed for use with rabbit polyclonal and monoclonal antibodies, this affinity purified goat anti-rabbit IgG (heavy and light chain) antibody is conjugated to horseradish peroxidase(HRP) for chemiluminescent detection.  This product is thoroughly validated with CST primary antibodies and will work optimally with the CST western immunoblotting protocol, ensuring accurate and reproducible results.
APPLICATIONS

Application Methods: Western Blotting

Background: Chemiluminescence systems have emerged as the best all-around method for western blot detection. They eliminate the hazards associated with radioactive materials and toxic chromogenic substrates. The speed and sensitivity of these methods are unequalled by traditional alternatives, and because results are generated on film, it is possible to record and store data permanently. Blots detected with chemiluminescent methods are easily stripped for subsequent reprobing with additional antibodies. HRP-conjugated secondary antibodies are utilized in conjunction with specific chemiluminescent substrates to generate the light signal. HRP conjugates have a very high turnover rate, yielding good sensitivity with short reaction times.

$121
250 µl
Anti-rat IgG (H+L) antibody was conjugated to Alexa Fluor® 488 fluorescent dye under optimal conditions and formulated at 2 mg/ml. This product has been optimized for use as a secondary antibody in immunofluorescent applications. Cell Signaling Technology’s strict quality control procedures assure that each conjugate provides optimal specificity and fluorescence.
APPLICATIONS

Application Methods: Immunofluorescence (Immunocytochemistry)

$121
250 µl
Anti-rat IgG (H+L) antibody was conjugated to Alexa Fluor® 555 fluorescent dye under optimal conditions and formulated at 2 mg/mL.
APPLICATIONS

Application Methods: Immunofluorescence (Immunocytochemistry)

$121
250 µl
Anti-rat IgG (H+L) was conjugated to Alexa Fluor® 647 fluorescent dye under optimal conditions and formulated at 2 mg/ml.
APPLICATIONS

Application Methods: Flow Cytometry, Immunofluorescence (Immunocytochemistry)

$142
1 ml
Affinity purified goat anti-rat IgG (heavy and light chain) antibody is conjugated to horseradish peroxidase(HRP) for chemiluminescent detection.  This product is thoroughly validated with CST primary antibodies and will work optimally with the CST western immunoblotting protocol, ensuring accurate and reproducible results.
APPLICATIONS
REACTIVITY
All Species Expected

Application Methods: Western Blotting

Background: Chemiluminescence systems have emerged as the best all-around method for western blot detection. They eliminate the hazards associated with radioactive materials and toxic chromogenic substrates. The speed and sensitivity of these methods are unequalled by traditional alternatives, and because results are generated on film, it is possible to record and store data permanently. Blots detected with chemiluminescent methods are easily stripped for subsequent reprobing with additional antibodies. HRP-conjugated secondary antibodies are utilized in conjunction with specific chemiluminescent substrates to generate the light signal. HRP conjugates have a very high turnover rate, yielding good sensitivity with short reaction times.

$146
100 µl
Affinity purified mouse anti-rabbit IgG (Conformation Specific) antibody. This product has been optimized for use as a secondary antibody in Western blotting applications.
APPLICATIONS

Application Methods: Western Blotting

$172
100 µl
Affinity purified mouse anti-rabbit IgG (Conformation Specific) HRP Conjugate antibody.
APPLICATIONS
REACTIVITY
All Species Expected

Application Methods: Western Blotting

$178
100 µl
APPLICATIONS

Application Methods: Western Blotting

$142
100 µl
This Cell Signaling Technology antibody is conjugated to the carbohydrate groups of horseradish peroxidase (HRP) via its amine groups.
APPLICATIONS

Application Methods: Western Blotting

$172
100 µl
This Cell Signaling Technology antibody is conjugated to the carbohydrate groups of horseradish peroxidase (HRP) via its amine groups.
APPLICATIONS

Application Methods: Western Blotting

$39
1 ml
$367
15 ml
SignalStain® Boost IHC Detection Reagent (HRP, Mouse) is a ready-to-use solution intended for use in immunohistochemical assays to detect mouse primary antibodies. SignalStain® Boost IHC Detection Reagent (HRP, Mouse) is a highly sensitive, one-step, polymer-based detection reagent that is specific for mouse IgG. It can be used to visualize targets in both paraffin-embedded and frozen tissue sections and it is compatible with all peroxidase-based substrates.
APPLICATIONS

Application Methods: Immunohistochemistry (Paraffin)

$39
1 ml
$367
15 ml
SignalStain® Boost IHC Detection Reagent (HRP, Rabbit) is a ready-to-use solution intended for use in immunohistochemical assays to detect rabbit primary antibodies. SignalStain® Boost IHC Detection Reagent (HRP, Rabbit) is a highly sensitive, one-step, polymer-based detection reagent that is specific for rabbit IgG. It can be used to visualize targets in both paraffin-embedded and frozen tissue sections and it is compatible with all peroxidase-based substrates.
APPLICATIONS

Application Methods: Immunohistochemistry (Paraffin)

$116
0.5nmol
60 µl
RNA interference is a method whereby gene expression can be selectively silenced through the delivery of double-stranded RNA molecules into the cell. SignalSilence® Control siRNA (Cy3® Conjugate) from Cell Signaling Technology (CST) is an siRNA sequence that will not lead to the specific degradation of any cellular message. It is intended to serve as a negative control for experiments using targeted siRNA transfection. In addition, this siRNA is Cy3®-conjugated to allow the researcher to assess transfection efficiency by fluorescence microscopy.
$116
0.5nmol
60 µl
RNA interference is a method whereby gene expression can be selectively silenced through the delivery of double-stranded RNA molecules into the cell. SignalSilence® Control siRNA (Cy5® Conjugate) from Cell Signaling Technology (CST) is an siRNA sequence that will not lead to the specific degradation of any cellular message. It is intended to serve as a negative control for experiments using targeted siRNA transfection. In addition, this siRNA is Cy5®-conjugated to allow the researcher to assess transfection efficiency by fluorescence microscopy.
$116
0.5nmol
60 µl
RNA interference is a method whereby gene expression can be selectively silenced through the delivery of double stranded RNA molecules into the cell. SignalSilence® Control siRNA (Fluorescein Conjugate) from Cell Signaling Technology (CST) is an siRNA sequence that will not lead to the specific degradation of any cellular message. It is intended to serve as a negative control for experiments using targeted siRNA transfection. In addition, this siRNA is fluorescein-conjugated to allow the researcher to assess transfection efficiency by fluorescence microscopy.
REACTIVITY
All Species Expected, All Species Expected, Human
$116
1.5 nmol
150 µl
RNA interference is a method whereby gene expression can be selectively silenced through the delivery of double stranded RNA molecules into the cell. The introduction of a specific small interfering RNA (siRNA) strand prevents the translation of a target protein message through RNA degradation. SignalSilence® Control siRNA (Unconjugated) is a siRNA sequence that will not lead to the specific degradation of any cellular message. It is intended to serve as a negative control for experiments using targeted siRNA transfection. This duplex contains the same scrambled sequence used in SignalSilence® Control siRNA (Fluorescein Conjugate) #6201.
REACTIVITY
All Species Expected
$54
1 liter
Tris buffered saline (TBS) solution for use as the blocking buffer diluent during fluorescent western blotting. Tween 20® detergent cannot be present in the blocking buffer because it can auto-fluoresce and increase non-specific background. After the blocking step, Tween 20® can be re-introduced to subsequent diluent buffers. Chemliluminescent western blotting does not require Tween 20® omission during blocking. Product is shipped and stored at room temperature.1X Formulation: 137 mM Sodium Chloride, 20 mM Tris. Supplied at pH 7.6.NOTE: This product does not contain Tween 20® detergent.
APPLICATIONS

Application Methods: Immunohistochemistry (Frozen)

$63
1000 ml
Tris buffered saline (TBS) solution with the detergent Tween® 20 for use as a wash buffer during western blotting. Product is shipped and stored at room temperature. 1X Formulation: 137 mM Sodium Chloride, 20 mM Tris, 0.1% Tween-20. Supplied at pH 7.6.
APPLICATIONS
REACTIVITY
All Species Expected

Application Methods: Immunohistochemistry (Paraffin), Western Blotting, Western Blotting

$61
1000 ml
Tris-Glycine SDS Running Buffer (10X) is used as the electrophoresis buffer during the stacking and resolve process of sodium dodecyl sulfate - polyacrylamide gel electrophoresis (SDS-PAGE). Product is shipped and stored at room temperature. 1X formulation: 25 mM Tris, 192 mM Glycine, 0.1% SDS, pH 8.3.
APPLICATIONS
REACTIVITY
All Species Expected

Application Methods: Western Blotting