Anti-Collagen III antibody [EPR17673] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal Collagen III antibody. Carrier free. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples.
View Alternative Names
Collagen alpha-1(III) chain, COL3A1
- IP
Lab
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993). Collagen III was immunoprecipitated from 0.35 mg of HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate with ab184993 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab184993 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/5000 dilution. Lane 1 : HeLa whole cell lysate 10 µg (Input). Lane 2 : ab184993 IP in HeLa whole cell lysate . Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab184993 in HeLa whole cell lysate . Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 5.5 seconds.
All lanes:
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>)
Lane 1:
HeLa whole cell lysate 10 µg (Input)
Lane 2:
HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 5.5s
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using ab184993, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized PC-12 (rat adrenal gland pheochromocytoma small irregularly shaped cells) cell line labeling Collagen III with ab184993 at 1/50 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed secondary antibody (ab150081) at 1/1000 dilution (green).Confocal image showing cytoplasmic staining in PC-12 cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution. Secondary antibody only control : Used PBS instead of primary antibody, secondary is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed secondary antibody (ab150081) at 1/1000 dilution. This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993). Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized PC-12 (Rat adrenal gland pheochromocytoma) cell line labeling Collagen III with ab184993 at 1/500 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488) (ab150081) at 1/2000 dilution was used as the secondary antibody.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993). Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cell line labeling Collagen III with ab184993 at 1/500 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488) (ab150081) at 1/2000 dilution was used as the secondary antibody.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using ab184993, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) cell line labeling Collagen III with ab184993 at 1/50 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed secondary antibody (ab150081) at 1/1000 dilution (green). Confocal image showing cytoplasmic staining in RAW 264.7 cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution. Secondary antibody only control : Used PBS instead of primary antibody, secondary is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed secondary antibody (ab150081) at 1/1000 dilution.
- IP
Lab
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993). Collagen III was immunoprecipitated from 0.35 mg of RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate with ab184993 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab184993 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/5000 dilution. Lane 1 : RAW 264.7 whole cell lysate 10 μg (Input). Lane 2 : ab184993 IP in RAW 264.7 whole cell lysate. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab184993 in RAW 264.7 whole cell lysate. Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 3.25 seconds. Lysate was freshly made and used immediately to minimize protein degradation.
All lanes:
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>)
Lane 1:
RAW 264.7 whole cell lysate 10 μg (Input).
Lane 2:
RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 3.25s
- IP
Lab
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993). Collagen III was immunoprecipitated from 0.35 mg of PC-12 (rat adrenal gland pheochromocytoma cell), whole cell lysate with ab184993 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab184993 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/5000 dilution. Lane 1 : PC-12 whole cell lysate 10 μg (Input). Lane 2 : ab184993 IP in PC-12 whole cell lysate. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab184993 in PC-12 whole cell lysate. Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 3.25 seconds. Lysate was freshly made and used immediately to minimize protein degradation.
All lanes:
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>) at 1/1000 dilution
Lane 1:
PC-12 whole cell lysate 10 μg (Input).
Lane 2:
PC-12 (rat adrenal gland pheochromocytoma cell), whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 3s
- WB
Supplier Data
Western blot - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using ab184993, the same antibody clone in a different buffer formulation. Exposure time : Lanes 1-3 : 30 seconds; Lane 4 : 5 seconds.
Blocking/Dilution buffer : 5% NFDM/TBST.
The molecular weight observed is consistent with what has been described in the literature (PMID : 26017148).
All lanes:
Western blot - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>) at 1/1000 dilution
Lane 1:
Human skin lysate at 10 µg
Lane 2:
Human skeletal muscle lysate at 10 µg
Lane 3:
Human heart lysate at 10 µg
Lane 4:
A431 (human epidermoid carcinoma cell line) whole cell lysate at 10 µg
Secondary
Lane 1:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Lanes 2 - 4:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 139 kDa
Observed band size: 150 kDa
true
- WB
Supplier Data
Western blot - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using ab184993, the same antibody clone in a different buffer formulation. Exposure time : Lane 1 : 3 minutes; Lane 2 : 15 seconds; Lane 3 : 3 seconds; Lanes 4-5 : 30 seconds.
Blocking/Dilution buffer : 5% NFDM/TBST.
The molecular weight observed is consistent with what has been described in the literature (PMID : 26017148).
All lanes:
Western blot - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>) at 1/1000 dilution
Lane 1:
Human fetal liver lysate at 20 µg
Lane 2:
Human fetal kidney lysate at 20 µg
Lane 3:
HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 4:
MCF7 (human breast adenocarcinoma cell line) whole cell lysate at 20 µg
Lane 5:
HaCaT (human keratinocyte cell line) whole cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 139 kDa
Observed band size: 150 kDa
true
- WB
Lab
Western blot - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
Blocking buffer and concentration : 5% NFDM/TBST Diluting buffer and concentration : 5% NFDM/TBST This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993).
All lanes:
Western blot - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>) at 1/1000 dilution
Lane 1:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 2:
Mouse heart tissue lysate at 20 µg
Lane 3:
Rat skeletal muscle tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 139 kDa
Observed band size: 150 kDa
true
Exposure time: 3min
- WB
Lab
Western blot - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
This data was developed using ab184993, the same antibody clone in a different buffer formulation. Exposure time : Lanes 1-4 : 92 seconds; Lanes 5-6 : 48 seconds; Lane 7 : 37 seconds. Blocking/Dilution buffer : 5% NFDM/TBST. In lane 1-4, the lysates were stored at -80℃ prior to Western Blotting. In lane 5-7, the lysates were freshly made and used for Western Blotting immediately to minimize protein degradation. This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993).
All lanes:
Western blot - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>) at 1/1000 dilution
Lane 1:
C6 (rat glial tumor glial cell), whole cell lysate at 20 µg
Lane 2:
RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate at 20 µg
Lane 3:
PC-12 (rat adrenal gland pheochromocytoma), whole cell lysate at 20 µg
Lane 4:
NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 20 µg
Lane 5:
C6 (rat glial tumor glial cell), whole cell fresh lysate at 20 µg
Lane 6:
RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell fresh lysate at 20 µg
Lane 7:
PC-12 (rat adrenal gland pheochromocytoma), whole cell fresh lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 139 kDa
Observed band size: 150 kDa
false
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (human epithelial cell line from cervix adenocarcinoma) cells labeling Collagen III with ab184993 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on HeLa cells.
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993).
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized MCF7 (human breast adenocarcinoma cell line) cells labeling Collagen III with ab184993 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on MCF7 cells.
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993).
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized HeLa (human epithelial cell line from cervix adenocarcinoma) cell line labeling Collagen III with ab184993 at 1/50 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993).
- IP
Supplier Data
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] - BSA and Azide free (AB224532)
Collagen III was immunoprecipitated from 0.35 mg of HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate with ab184993 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab184993 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution.
Lane 1 : HeLa whole cell lysate 10 μg (Input).
Lane 2 : ab184993 IP in HeLa whole cell lysate .
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab184993 in HeLa whole cell lysate .
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab184993).
All lanes:
Immunoprecipitation - Anti-Collagen III antibody [EPR17673] (<a href='/en-us/products/primary-antibodies/collagen-iii-antibody-epr17673-ab184993'>ab184993</a>)
Predicted band size: 139 kDa
Observed band size: 150 kDa
false
Related conjugates and formulations (3)
-
Anti-Collagen III antibody [EPR17673]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-Collagen III antibody [EPR17673]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-Collagen III antibody [EPR17673]
Reactivity data
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Why is this recommended?
We recommend this product because it’s often used in the same experiment or related research.
We advise that you always check the datasheet to ensure it fits your experiments, or contact ourtechnical teamfor help.
Product details
ab224532 is the carrier-free version of ab184993.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
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.
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
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Collagen type III contributes to maintaining the structural integrity of tissues. It forms a complex with collagen type I providing a scaffold that ensures mechanical strength and stability to tissues. This structural pairing of collagen type I and III highlights their cooperative function in supporting the extracellular matrix and regulating cell behavior in tissue repair and wound healing processes.
Pathways
Collagen type III is integral to the processes of tissue repair and fibrosis pathways. It interacts closely with proteins such as fibronectin and integrins contributing to the cellular adhesion and signaling pathways important for fibroblast function and migration. These interactions reflect its essential role in matrix assembly and stability influencing how cells respond to injury and repair damaged tissues.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Product promise
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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