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AB255871

Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free

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(1 Publication)

Rat Recombinant Monoclonal Serum Response Factor SRF antibody. Carrier free. Suitable for IP, WB, IHC-P and reacts with Mouse, Human, Rat samples. Cited in 1 publication.

View Alternative Names

Serum response factor, SRF

7 Images
Immunoprecipitation - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)
  • IP

Lab

Immunoprecipitation - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)

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).

All lanes:

Immunoprecipitation - Anti-Serum Response Factor SRF antibody [2C5] (<a href='/en-us/products/primary-antibodies/serum-response-factor-srf-antibody-2c5-ab252868'>ab252868</a>) at 1/1000 dilution

Predicted band size: 52 kDa

Observed band size: 57 kDa,67 kDa

false

Exposure time: 6s

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)

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).

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)

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).

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)

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).

Immunoprecipitation - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)
  • IP

Lab

Immunoprecipitation - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)

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).

All lanes:

Immunoprecipitation - Anti-Serum Response Factor SRF antibody [2C5] (<a href='/en-us/products/primary-antibodies/serum-response-factor-srf-antibody-2c5-ab252868'>ab252868</a>) at 1/1000 dilution

Predicted band size: 52 kDa

Observed band size: 57 kDa,67 kDa

false

Exposure time: 6s

Western blot - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)
  • WB

Lab

Western blot - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)

Blocking/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).

All lanes:

Western blot - Anti-Serum Response Factor SRF antibody [2C5] (<a href='/en-us/products/primary-antibodies/serum-response-factor-srf-antibody-2c5-ab252868'>ab252868</a>) at 1.082 µg/mL

Lane 1:

HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 10 µg

Lane 2:

HEK-293 (human embryonic kidney epithelial cell), whole cell lysate at 10 µg

Lane 3:

K562 (human chronic myelogenous leukemia lymphoblast), whole cell lysate at 10 µg

Lane 4:

C2C12 (mouse myoblasts myoblast), whole cell lysate at 10 µg

Secondary

All lanes:

Western blot - Goat Anti-Rat IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rat-igg-h-l-hrp-ab205720'>ab205720</a>) at 1/5000 dilution

Predicted band size: 52 kDa

Observed band size: 52 kDa,57 kDa,67 kDa

false

Exposure time: 20s

Western blot - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)
  • WB

Lab

Western blot - Anti-Serum Response Factor SRF antibody [2C5] - BSA and Azide free (AB255871)

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).

All lanes:

Western blot - Anti-Serum Response Factor SRF antibody [2C5] (<a href='/en-us/products/primary-antibodies/serum-response-factor-srf-antibody-2c5-ab252868'>ab252868</a>) at 0.082 µg/mL

Lane 1:

NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 10 µg

Lane 2:

PC-12 (rat adrenal gland pheochromocytoma), whole cell lysate at 10 µg

Secondary

All lanes:

Western blot - Goat Anti-Rat IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rat-igg-h-l-hrp-ab205720'>ab205720</a>) at 1/5000 dilution

Predicted band size: 52 kDa

Observed band size: 52 kDa,57 kDa,67 kDa

false

  • Unconjugated

    Anti-Serum Response Factor SRF antibody [2C5]

Key facts

Host species

Rat

Clonality

Monoclonal

Clone number

2C5

Isotype

IgG2a

Light chain type

kappa

Carrier free

Yes

Reacts with

Mouse, Rat, Human

Applications

IP, IHC-P, WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "IP" : {"fullname" : "Immunoprecipitation", "shortname":"IP"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"}, "IHCP" : {"fullname" : "Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)", "shortname":"IHC-P"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "IP-species-checked": "testedAndGuaranteed", "IP-species-dilution-info": "", "IP-species-notes": "<p></p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "", "WB-species-notes": "<p></p>", "IHCP-species-checked": "notRecommended", "IHCP-species-dilution-info": "", "IHCP-species-notes": "<p></p>" }, "Mouse": { "IP-species-checked": "testedAndGuaranteed", "IP-species-dilution-info": "", "IP-species-notes": "<p></p>", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "", "WB-species-notes": "<p></p>", "IHCP-species-checked": "testedAndGuaranteed", "IHCP-species-dilution-info": "", "IHCP-species-notes": "<p></p>" }, "Rat": { "IP-species-checked": "guaranteed", "IP-species-dilution-info": "", "IP-species-notes": "", "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "", "WB-species-notes": "<p></p>", "IHCP-species-checked": "testedAndGuaranteed", "IHCP-species-dilution-info": "", "IHCP-species-notes": "<p></p>" } } }

Product details

ab255871 is the carrier-free version of ab252868.

What are the advantages of a recombinant monoclonal antibody?
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 batch production

For more information, read more on recombinant antibodies.

Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com

Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.

Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.

Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
Do Not Freeze

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Serum Response Factor (SRF) also known as serum response element-binding protein is a transcription factor with a mass of around 67 kDa. SRF regulates gene expression by binding to the serum response element (SRE) found in the promoter region of target genes. It is widely expressed across multiple tissues including muscle brain and epithelial cells. SRF plays a critical role in various cellular functions due to its ability to control the transcription of immediate-early genes in response to a range of extracellular signals.
Biological function summary

SRF influences cellular processes such as growth differentiation and migration. SRF often functions as a part of a transcriptional complex interacting with co-factors like the ternary complex factor (TCF) from the ETS domain family of transcription factors. This interaction modulates the expression of genes involved in cytoskeletal organization and cell cycle regulation. By doing so SRF coordinates complex cellular activities that are essential for normal development and response to environmental changes.

Pathways

SRF plays a significant role in the mitogen-activated protein kinase (MAPK) pathway and the RhoA pathway. In the MAPK pathway SRF acts downstream to mediate the response of cells to growth stimuli working closely with MAPK-regulated kinases. Through the RhoA pathway SRF regulates changes in cytoskeletal dynamics and cell movement with the involvement of proteins such as Rho-associated coiled-coil containing protein kinase (ROCK) and myocardin-related transcription factors (MRTFs).

SRF has a strong connection to cardiovascular diseases and certain types of cancer. Alterations in SRF expression or function can contribute to the development of atherosclerosis and myocardial hypertrophy. Additionally dysregulation in SRF activity has been observed in some cancers where it associates with aberrant cell proliferation and migration. In these contexts proteins such as connective tissue growth factor (CTGF) can interact with SRF further impacting disease progression and severity.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

SRF is a transcription factor that binds to the serum response element (SRE), a short sequence of dyad symmetry located 300 bp to the 5' of the site of transcription initiation of some genes (such as FOS). Together with MRTFA transcription coactivator, controls expression of genes regulating the cytoskeleton during development, morphogenesis and cell migration. The SRF-MRTFA complex activity responds to Rho GTPase-induced changes in cellular globular actin (G-actin) concentration, thereby coupling cytoskeletal gene expression to cytoskeletal dynamics. Required for cardiac differentiation and maturation.
See full target information Serum response factor

Publications (1)

Recent publications for all applications. Explore the full list and refine your search

The Journal of clinical investigation 119:899-910 PubMed19307725

2009

Loss of serum response factor in keratinocytes results in hyperproliferative skin disease in mice.

Applications

Unspecified application

Species

Unspecified reactive species

Heidi Koegel,Lukas von Tobel,Matthias Schäfer,Siegfried Alberti,Elisabeth Kremmer,Cornelia Mauch,Daniel Hohl,Xiao-Jing Wang,Hans-Dietmar Beer,Wilhelm Bloch,Alfred Nordheim,Sabine Werner
View all publications

Product promise

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