Name: Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free
SKU: ab234965
Rating: 4 (1 reviews)

Anti-PDGFR alpha [EPR22059-270] antibody (ab234965) is a rabbit monoclonal antibody that is provided in a PBS only formulation free from BSA and azide. Formulated to be conjugation-ready. It is used to detect PDGFR alpha in Western Blot, Flow Cytometry, IP, IHC-P, IHC-Fr, ICC/IF, ELISA. Suitable for Human, Mouse, Rat samples.

- Specificity confirmed with PDGFR alpha knockout cell line validation
-BSA, sodium azide, and glycerol-free for consistent conjugation with fluorochromes, enzymes and more

Images

Flow Cytometry - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (AB234965), expandable thumbnail

Publications

Key facts

Isotype: IgG
Host species: Rabbit
Storage buffer: pH: 7.2 - 7.4
Constituents: PBS
Form: Liquid
Clonality: Monoclonal

Immunogen

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

Reactivity data

Select an application

Product promiseTestedExpectedPredictedNot recommended

	IP	Flow Cyt	I-ELISA	WB	ICC/IF	IHC-Fr	IHC-P
Human	Tested	Tested	Expected	Tested	Tested	Tested	Tested
Mouse	Expected	Tested	Expected	Tested	Expected	Expected	Tested
Rat	Expected	Expected	Expected	Tested	Expected	Expected	Tested
Recombinant full length protein - Human	Not recommended	Not recommended	Tested	Not recommended	Not recommended	Not recommended	Not recommended

Tested
Tested

Species	Dilution info	Notes
Species Human	Dilution info -	Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Expected
Expected

Species	Dilution info	Notes
Species Mouse, Rat	Dilution info Use at an assay dependent concentration.	Notes -

Not recommended
Not recommended

Species	Dilution info	Notes
Species Recombinant full length protein - Human	Dilution info -	Notes -

Tested
Tested

Species	Dilution info	Notes
Species Mouse	Dilution info -	Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Species Human	Dilution info -	Notes -

Expected
Expected

Species	Dilution info	Notes
Species Rat	Dilution info Use at an assay dependent concentration.	Notes -

Not recommended
Not recommended

Species	Dilution info	Notes
Species Recombinant full length protein - Human	Dilution info -	Notes -

Tested
Tested

Species	Dilution info	Notes
Species Recombinant full length protein - Human	Dilution info 1 µg/mL	Notes -

Expected
Expected

Species	Dilution info	Notes
Species Human, Mouse, Rat	Dilution info Use at an assay dependent concentration.	Notes -

Tested
Tested

Species	Dilution info	Notes
Species Mouse, Rat, Human	Dilution info -	Notes -

Not recommended
Not recommended

Species	Dilution info	Notes
Species Recombinant full length protein - Human	Dilution info -	Notes -

Tested
Tested

Species	Dilution info	Notes
Species Human	Dilution info -	Notes -

Expected
Expected

Species	Dilution info	Notes
Species Mouse, Rat	Dilution info Use at an assay dependent concentration.	Notes -

Not recommended
Not recommended

Species	Dilution info	Notes
Species Recombinant full length protein - Human	Dilution info -	Notes -

Tested
Tested

Species	Dilution info	Notes
Species Human	Dilution info -	Notes -

Expected
Expected

Species	Dilution info	Notes
Species Mouse, Rat	Dilution info Use at an assay dependent concentration.	Notes -

Not recommended
Not recommended

Species	Dilution info	Notes
Species Recombinant full length protein - Human	Dilution info -	Notes -

Tested
Tested

Species	Dilution info	Notes
Species Human	Dilution info -	Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Species Mouse	Dilution info -	Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Species Rat	Dilution info -	Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Not recommended
Not recommended

Species	Dilution info	Notes
Species Recombinant full length protein - Human	Dilution info -	Notes -

Associated Products

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2 products for Alternative Version

Target data

See full target information PDGFRA

Function

Tyrosine-protein kinase that acts as a cell-surface receptor for PDGFA, PDGFB and PDGFC and plays an essential role in the regulation of embryonic development, cell proliferation, survival and chemotaxis. Depending on the context, promotes or inhibits cell proliferation and cell migration. Plays an important role in the differentiation of bone marrow-derived mesenchymal stem cells. Required for normal skeleton development and cephalic closure during embryonic development. Required for normal development of the mucosa lining the gastrointestinal tract, and for recruitment of mesenchymal cells and normal development of intestinal villi. Plays a role in cell migration and chemotaxis in wound healing. Plays a role in platelet activation, secretion of agonists from platelet granules, and in thrombin-induced platelet aggregation. Binding of its cognate ligands - homodimeric PDGFA, homodimeric PDGFB, heterodimers formed by PDGFA and PDGFB or homodimeric PDGFC -leads to the activation of several signaling cascades; the response depends on the nature of the bound ligand and is modulated by the formation of heterodimers between PDGFRA and PDGFRB. Phosphorylates PIK3R1, PLCG1, and PTPN11. Activation of PLCG1 leads to the production of the cellular signaling molecules diacylglycerol and inositol 1,4,5-trisphosphate, mobilization of cytosolic Ca(2+) and the activation of protein kinase C. Phosphorylates PIK3R1, the regulatory subunit of phosphatidylinositol 3-kinase, and thereby mediates activation of the AKT1 signaling pathway. Mediates activation of HRAS and of the MAP kinases MAPK1/ERK2 and/or MAPK3/ERK1. Promotes activation of STAT family members STAT1, STAT3 and STAT5A and/or STAT5B. Receptor signaling is down-regulated by protein phosphatases that dephosphorylate the receptor and its down-stream effectors, and by rapid internalization of the activated receptor.

Alternative names

CD140a, PDGFR2, RHEPDGFRA, PDGFRA, Platelet-derived growth factor receptor alpha, PDGF-R-alpha, PDGFR-alpha, Alpha platelet-derived growth factor receptor, Alpha-type platelet-derived growth factor receptor, CD140 antigen-like family member A, CD140a antigen, Platelet-derived growth factor alpha receptor, Platelet-derived growth factor receptor 2, PDGFR-2

Key facts

Isotype: IgG
Host species: Rabbit
Storage buffer: pH: 7.2 - 7.4
Constituents: PBS
Form: Liquid
Clonality: Monoclonal
Immunogen: The exact immunogen used to generate this antibody is proprietary information.
Carrier free: Yes
Clone number: EPR22059-270
Purification technique: Affinity purification Protein A
Specificity: PDGFR alpha is membrane protein, so enrichment of membrane could help increasing the detection level of PDGFR alpha.
Concentration

Storage

Shipped at conditions: Blue Ice
Appropriate short-term storage conditions: +4°C
Appropriate long-term storage conditions: +4°C
Storage information: Do Not Freeze

Notes

What is this antibody validated in?

Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Flow Cytometry (Flow Cyt), Immunoprecipitation (IP), Immunohistochemistry (IHC-P), Immunohistochemistry (IHC-Fr), Immunocytochemistry/immunofluorescence (ICC/IF), ELISA in Human, Mouse, Rat samples.

What is the molecular weight of PDGFR alpha?

Anti-PDGFR alpha [EPR22059-270] - BSA and Azide free (ab234965) specifically detects a band for PDGFR alpha (UniProt: P16234) at a molecular weight of 122kDa.

Specificity confirmed

The specificity of Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965) has been confirmed by Western blot testing in PDGFRA Knockout SH-SY5Y cell line.

Other related products

We have a range of other formats of antibody clone [EPR22059-270] also available for your convenience:
ab203491, Carrier free - ab234965, Alexa Fluor® 647 - ab270085, PE - ab270086, Alexa Fluor® 488 - ab307855

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.

Supplementary info

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

Activity summary

PDGFR alpha also known as platelet-derived growth factor receptor alpha is a cell surface receptor tyrosine kinase with a mass of approximately 123 kDa. It plays a mechanical role in transmitting signals across the cell membrane initiating cellular responses. PDGFR alpha is widely expressed in mesenchymal cells including fibroblasts and smooth muscle cells. Researchers frequently employ techniques such as PDGFRA IHC and PDGFRA staining to study the localization and expression levels in tissues.

Biological function summary

PDGFR alpha mediates cell proliferation survival and differentiation especially in embryonic development and wound healing. The receptor often forms a complex by dimerizing with itself or with PDGFR beta to activate intracellular signaling cascades. This process is initiated upon ligand binding which triggers autophosphorylation on tyrosine residues. The receptor is also recognized in the detection of PDGFRA with assays such as PDGFRA ELISA.

Pathways

PDGFR alpha significantly affects the MAPK and PI3K/AKT signaling pathways which regulate cellular growth and survival signals. Through these pathways PDGFR alpha interacts with related proteins like SHP-2 and PI3K contributing to signal transduction involved in cellular responses. This role links PDGFR alpha to important cellular processes via its kinase activity and signal integration.

Associated diseases and disorders

PDGFR alpha is implicated in conditions such as gastrointestinal stromal tumors (GISTs) and idiopathic pulmonary fibrosis (IPF). It connects to proteins such as KIT in GISTs where mutations cause aberrant receptor signaling leading to tumorigenesis. Aberrant PDGFR alpha signaling also associates with IPF a disorder characterized by increased fibroblast proliferation and fibrotic tissue formation. These connections make PDGFR alpha a significant target for research and therapeutic intervention.

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

Full details and terms and conditions can be found here:
Terms & Conditions.

15 product images

Flow Cytometry - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Flow cytometric analysis of NIH/3T3 (mouse embyro fibroblast cell line) cell line labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/500 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (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) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution was used as the secondary antibody.
Gated on viable cells.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Immunoprecipitation - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
PDGFR alpha was immunoprecipitated from 0.35 mg of A-204 (human muscle rhabdomyosarcoma cell line) whole cell lysate with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/30 dilution. Western blot was performed from the immunoprecipitate using Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366), was used for detection at 1/1000 dilution.
Lane 1: A-204 whole cell lysate 10 μg (Input).
Lane 2: Anti-PDGFR alpha antibody [EPR22059-270] ab203491 IP in A-204 whole cell lysate.
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-PDGFR alpha antibody [EPR22059-270] ab203491 in A-204 whole cell lysate.
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 50 seconds.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
All lanes: Immunoprecipitation - Anti-PDGFR alpha antibody [EPR22059-270] (Anti-PDGFR alpha antibody [EPR22059-270] ab203491)
Predicted band size: 122 kDa
Observed band size: 150 kDa, 180 kDa
Western blot - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
This data was developed using the same antibody clone in a different buffer formulation (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Lanes 1 - 2: Merged signal (red and green). Green - Anti-PDGFR alpha antibody [EPR22059-270] ab203491 observed at 150 kDa. Red - loading control Anti-GAPDH antibody [6C5] - Loading Control ab8245 (Mouse anti-GAPDH antibody [6C5]) observed at 37 kDa.
Anti-PDGFR alpha antibody [EPR22059-270] ab203491 was shown to react with PDGFR alpha in wild-type SH-SY5Y cells in Western blot with loss of signal observed in PDGFRA knockout sample. Wild-type SH-SY5Y and PDGFRA knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3 % milk in TBS-T (0.1 % Tween^®) before incubation with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 and Anti-GAPDH antibody [6C5] - Loading Control ab8245 (Mouse anti-GAPDH antibody [6C5]) overnight at 4 °C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preabsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preabsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) secondary antibodies at 1 in 20000 dilution for 1 h at room temperature before imaging.
All lanes: Western blot - Anti-PDGFR alpha antibody [EPR22059-270] (Anti-PDGFR alpha antibody [EPR22059-270] ab203491) at 1/1000 dilution
Lane 1: Wild-type SH-SY5Y cell lysate at 40 µg
Lane 2: PDGFRA knockout SH-SY5Y cell lysate at 40 µg
Lane 2: Western blot - Human PDGFRA knockout SH-SY5Y cell line (Human PDGFRA knockout SH-SY5Y cell line ab275335)
Performed under reducing conditions.
Predicted band size: 122 kDa
Observed band size: 150 kDa
Immunocytochemistry/ Immunofluorescence - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
This data was developed using the same antibody clone in a different buffer formulation (Anti-PDGFR alpha antibody [EPR22059-270] ab203491) (Human PDGFRA knockout SH-SY5Y cell line ab275335). Anti-PDGFR alpha antibody [EPR22059-270] ab203491 staining PDGFR alpha in wild-type SH-SY5Y cells (top panel) and PDGFRA knockout SH-SY5Y cells (bottom panel). The cells were fixed with 100% methanol (5 min) then permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1μg/ml concentration and Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (Mouse monoclonal to alpha Tubulin) at 1/1000 dilution overnight at 4°C followed by a further incubation at room temperature for 1h with a goat secondary antibody to rabbit IgG (Alexa Fluor^® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 2 μg/ml (shown in green) and a goat secondary antibody to mouse IgG (Alexa Fluor^® 594) (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at 2 μg/ml (shown in red). Nuclear DNA was labelled in blue with DAPI.
Image was taken with a confocal microscope (Leica-Microsystems TCS SP8).
Immunocytochemistry/ Immunofluorescence - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized A-204 (human muscle rhabdomyosarcoma cell line) cells and A-172 (human brain glioblastoma cell line) labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/1000 dilution (green).
Confocal image showing membranous and cytoplasmic staining in A-204 cell line.
Negative control: A-172 (PMID:8425771.
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor^® 594) (Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker 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) (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 (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Flow Cytometry - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Flow cytometric analysis of A-172 (human brain glioblastoma cell line, left) and A-204 (human muscle rhabdomyosarcoma cell line, right) cell lines labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/50 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (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) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution was used as the secondary antibody.
Gated on viable cells.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Immunohistochemical analysis of paraffin-embedded mouse uterus tissue labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Positive staining on interstitial cells of mouse uterus (PMID: 25788664). Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Heat mediated antigen retrieval was performed with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Immunohistochemical analysis of paraffin-embedded rat E14.5 intervertebral disc tissue labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Positive staining in mesenchymal cells of rat E14.5 intervertebral disc (PMID: 9199674). Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Heat mediated antigen retrieval was performed with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Immunohistochemical analysis of paraffin-embedded mouse E14.5 lung tissue labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Positive staining in the mesenchyme of mouse E14.5 lung (PMID: 8681381). Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Heat mediated antigen retrieval was performed with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Immunohistochemical analysis of paraffin-embedded mouse E14.5 intervertebral disc tissue labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Positive staining in mesenchymal cells of mouse E14.5 intervertebral disc (PMID: 9199674). Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Heat mediated antigen retrieval was performed with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
Immunohistochemical analysis of paraffin-embedded human endometrium tissue labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 0.26 µg/mL followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining in human endometrium was observed. The section was incubated with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 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 a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins was used.

This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).

Immunohistochemical analysis of paraffin-embedded human human bladder carcinoma labeling PDGFR alpha with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at 0.26 µg/mL followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining in human bladder carcinoma was observed. The section was incubated with Anti-PDGFR alpha antibody [EPR22059-270] ab203491 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 a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins was used.
Indirect ELISA - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
indirect ELISA using Anti-PDGFR alpha antibody [EPR22059-270] ab203491 at varying antibody concentrations (4000~0 ng /ml) and Human PDGF Receptor alpha antigen at 1000 ng/ml. Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution dilution was used as a secondary antibody.This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).
Western blot - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
This data was developed using the same antibody clone in a different buffer formulation (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).

Blocking/Dilution buffer: 5% NFDM/TBST.

We recommend using higher sensitivity ECL to improve results.

Anti-PDGFR alpha antibody [EPR5480] ab134123 can be a good alternative when testing samples with low level of PDGFR alpha which detects stronger signal than Anti-PDGFR alpha antibody [EPR22059-270] ab203491 in western blot.
Lanes 1 - 10: Western blot - Anti-PDGFR alpha antibody [EPR22059-270] (Anti-PDGFR alpha antibody [EPR22059-270] ab203491) at 1/1000 dilution
Lanes 11 - 15: Western blot - Anti-PDGFR alpha antibody [EPR5480] (Anti-PDGFR alpha antibody [EPR5480] ab134123) at 1/1000 dilution
Lanes 1, 6 and 11: Rat heart tissue lysate at 20 µg
Lanes 2, 7 and 12: Rat lung tissue lysate at 20 µg
Lanes 3, 8 and 13: Mouse brain tissue lysate at 20 µg
Lanes 4, 9 and 14: Mouse heart tissue lysate at 20 µg
Lanes 5, 10 and 15: Mouse lung tissue lysate at 20 µg
Secondary
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 122 kDa
Observed band size: 150 kDa
Exposure time: 80s
Western blot - Anti-PDGFR alpha antibody [EPR22059-270] - BSA and Azide free (ab234965)
This data was developed using the same antibody clone in a different buffer formulation (Anti-PDGFR alpha antibody [EPR22059-270] ab203491).

Blocking/Dilution buffer: 5% NFDM/TBST.

We recommend using higher sensitivity ECL to improve results.

Anti-PDGFR alpha antibody [EPR5480] ab134123 can be a good alternative when testing samples with low level of PDGFR alpha which detects stronger signal than Anti-PDGFR alpha antibody [EPR22059-270] ab203491 in western blot.
Lanes 1 - 8: Western blot - Anti-PDGFR alpha antibody [EPR22059-270] (Anti-PDGFR alpha antibody [EPR22059-270] ab203491) at 1/1000 dilution
Lanes 9 - 12: Western blot - Anti-PDGFR alpha antibody [EPR5480] (Anti-PDGFR alpha antibody [EPR5480] ab134123) at 1/1000 dilution
Lanes 1, 5 and 9: SH-SY5Y
Lanes 2, 6 and 10: Human brain tissue lysate at 20 µg
Lanes 3, 7 and 11: Human heart tissue lysate at 20 µg
Lanes 4, 8 and 12: Human lung tissue lysate at 20 µg
Secondary
All lanes: Western blot at 1/2000 dilution
Predicted band size: 122 kDa
Observed band size: 150 kDa
Exposure time: 80s