Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (ab255871)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rat monoclonal [2C5] to Serum Response Factor SRF - BSA and Azide free
- Suitable for: IHC-P, IP, WB
- Reacts with: Mouse, Rat, Human
Overview
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Product name
Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free
See all Serum Response Factor SRF primary antibodies -
Description
Rat monoclonal [2C5] to Serum Response Factor SRF - BSA and Azide free -
Host species
Rat -
Tested applications
Suitable for: IHC-P, IP, WBmore details -
Species reactivity
Reacts with: Mouse, Rat, Human -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: HeLa, NIH/3T3, PC-12, HEK-293, K562 and C2C12 whole cell lysates. IP: HeLa and C2C12 whole cell lysates. IHC-P: Mouse cerebrum tissue. Mouse and rat skeletal muscle tissue.
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General notes
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.
ab255871 is the carrier-free version of ab252868. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
2C5 -
Isotype
IgG2a -
Light chain type
kappa -
Research areas
Images
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All lanes : Anti-Serum Response Factor SRF antibody [2C5] (ab252868) at 1.082 µg/ml
Lane 1 : NIH/3T3 (mouse embryonic fibroblast), whole cell lysate
Lane 2 : PC-12 (rat adrenal gland pheochromocytoma), whole cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rat IgG H&L (HRP) (ab205720) at 1/5000 dilution
Predicted band size: 52 kDa
Observed band size: 52,57,67 kDa why is the actual band size different from the predicted?Blocking/Dilution buffer: 5% NFDM/TBST.
Exposure times: Lane 1: 26 seconds; Lane 2: 3 minutes.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 11893590 and PMID: 10642500).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252868).
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Serum Response Factor SRF was immunoprecipitated from C2C12 (mouse myoblasts myoblast), whole cell lysate with ab252868 at 1/30 dilution (2µg in 0.35mg lysates) (36.067µg/ml). Western blot was performed on the immunoprecipitate using ab252868 at 1/1000 dilution. Goat Anti-rat IgG (H+L), HRP) (ab205720) was used at 1/10000 dilution.
Lane 1: C2C12 whole cell lysate 10µg.
Lane 2: ab252868 IP in C2C12 whole cell lysate.
Lane 3: Rat monoclonal IgG2a (ab18450) instead of ab252868 in C2C12 whole cell lysate.
Blocking/Dilution buffer: 5% NFDM/TBST.
Exposure time: 6 seconds.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 11893590 and PMID: 10642500).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252868).
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All lanes : Anti-Serum Response Factor SRF antibody [2C5] (ab252868) at 1.082 µg/ml
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate
Lane 2 : HEK-293 (human embryonic kidney epithelial cell), whole cell lysate
Lane 3 : K562 (human chronic myelogenous leukemia lymphoblast), whole cell lysate
Lane 4 : C2C12 (mouse myoblasts myoblast), whole cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rat IgG H&L (HRP) (ab205720) at 1/5000 dilution
Predicted band size: 52 kDa
Exposure time: 20 secondsBlocking/Dilution buffer: 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 11893590 and PMID: 10642500).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252868).
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Serum Response Factor SRF was immunoprecipitated from HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate with ab252868 at 1/30 dilution (2µg in 0.35mg lysates) (36.067µg/ml). Western blot was performed on the immunoprecipitate using ab252868 at 1/1000 dilution. Goat Anti-rat IgG (H+L), HRP) (ab205720) was used at 1/10000 dilution.
Lane 1: HeLa whole cell lysate 10µg.
Lane 2: ab252868 IP in HeLa whole cell lysate.
Lane 3: Rat monoclonal IgG2a (ab18450) instead of ab252868 in HeLa whole cell lysate.
Blocking/Dilution buffer: 5% NFDM/TBST.
Exposure time: 10 seconds.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 11893590and PMID: 10642500).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252868).
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Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling Serum Response Factor SRF with ab252868 at 1/1000 dilution (1.082µg/ml) followed by ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Nuclear staining on mouse cerebrum. The section was incubated with ab252868 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252868).
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Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue labeling Serum Response Factor SRF with ab252868 at 1/1000 dilution (1.082µg/ml) followed by ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Nuclear staining on mouse skeletal muscle tissue. The section was incubated with ab252868 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252868).
-
Immunohistochemical analysis of paraffin-embedded rat skeletal muscle tissue labeling Serum Response Factor SRF with ab252868 at 1/1000 dilution (1.082µg/ml) followed by ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Nuclear staining on rat skeletal muscle tissue. The section was incubated with ab252868 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252868).
-