Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal PDGFR beta antibody. Carrier free. Suitable for IP, ELISA, WB, IHC-P, IHC-FoFr, ICC/IF, Flow Cyt (Intra) and reacts with Mouse, Human samples.
View Alternative Names
CD140b, PDGFR, PDGFR1, PDGFRB, Platelet-derived growth factor receptor beta, PDGF-R-beta, PDGFR-beta, Beta platelet-derived growth factor receptor, Beta-type platelet-derived growth factor receptor, CD140 antigen-like family member B, Platelet-derived growth factor receptor 1, PDGFR-1, 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
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
ab32570 staining PDGFR alpha + beta in human breast tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Shows positive staining on stromal cells. Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0). Samples were incubated with primary antibody (1/500). An HRP-conjugated Goat anti-rabbit IgG (ready to use) was used as the secondary antibody. Counter stained with Hematoxylin.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32570).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
ab32570 staining PDGFR alpha + beta in human lung cancer tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Shows positive staining on stromal cells. Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0). Samples were incubated with primary antibody (1/500). An HRP-conjugated Goat anti-rabbit IgG (ready to use) was used as the secondary antibody. Counter stained with Hematoxylin.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32570).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
Immunohistochemical staining of paraffin embedded human spleen with purified ab32570 at a working dilution of 1/50. The secondary antibody used is ab97051, a HRP-conjugated goat anti-rabbit IgG (H+L), at a dilution of 1/500. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32570).
- ELISA
Supplier Data
ELISA - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32570).
ELISA showing primary antibody ab32570 binding to the antigen Human PDGFR alpha protein and Human PDGFR beta protein.
Primary antibody concentration ranges from 0 - 1000 ng/mL.
Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) was used as a secondary antibody at 1/2500 dilution.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
Intracellular Flow Cytometry analysis of NIH/3T3 (Mouse embryo fibroblast cell line) cells labeling PDGFR alpha + beta (red) with ab32570 at a 1/20 dilution. Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol. A goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) was used as the secondary antibody at a 1/2000 dilution. Black - Rabbit monoclonal IgG (ab172730). Blue (unlabeled control) - Cells without incubation with primary and secondary antibodies.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32570).
- IP
Unknown
Immunoprecipitation - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
ab32570 (purified) at 1/20 immunoprecipitating PDGFR alpha + beta in NIH/3T3 (Mouse embryo fibroblast cell line) (Lane 1 and 2). Lane 3 - PBS.
For western blotting a HRP-conjugated anti-rabbit IgG specific to the non-reduced form of IgG was used as the secondary antibody (1/1500).
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 (ab32570).
All lanes:
Immunoprecipitation - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - C-terminal (<a href='/en-us/products/primary-antibodies/pdgfr-alpha-pdgfr-beta-antibody-y92-c-terminal-ab32570'>ab32570</a>)
Observed band size: 175 kDa
false
- WB
Lab
Western blot - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
This data was developed using the same antibody clone in a different buffer formulation (ab32570).
Lanes 1 - 4 : Merged signal (red and green). Green - ab32570 observed at 170 kDa. Red - loading control ab7291 (Mouse anti-Alpha Tubulin [DM1A]) observed at 55 kDa.
ab32570 was shown to react with PDGFRB in wild-type SH-SY5Y cells in Western blot with loss of signal observed in PDGFRB knockout cell line ab273749 (knockout cell lysate ab275523). Wild-type SH-SY5Y and PDGFRB knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in fluorescent western blot (TBS-based) blocking solution before incubation with ab32570 and ab7291 (Mouse anti-Alpha Tubulin [DM1A]) overnight at 4 °C at a 1 in 5000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - C-terminal (<a href='/en-us/products/primary-antibodies/pdgfr-alpha-pdgfr-beta-antibody-y92-c-terminal-ab32570'>ab32570</a>) at 1/5000 dilution
Lane 1:
Wild-type SH-SY5Y cell lysate at 30 µg
Lane 2:
PDGFR beta knockout SH-SY5Y cell lysate at 30 µg
Lane 2:
Western blot - Human PDGFRB knockout SH-SY5Y cell line (<a href='/en-us/products/cell-lines/human-pdgfrb-knockout-sh-sy5y-cell-line-ab273749'>ab273749</a>)
Lane 3:
Human Skeletal Muscle tissue lysate at 30 µg
Lane 4:
HeLa cell lysate at 30 µg
Predicted band size: 123 kDa
Observed band size: 170 kDa
false
- WB
Lab
Western blot - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
This data was developed using ab32570, the same antibody clone in a different buffer formulation. Different batches of ab32570 were tested on Rat brain lysate at 1.0 µg/ml. 15 µg of lysate was loaded in each lane. Bands observed at 175 kDa.
All lanes:
Western blot - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - C-terminal (<a href='/en-us/products/primary-antibodies/pdgfr-alpha-pdgfr-beta-antibody-y92-c-terminal-ab32570'>ab32570</a>)
false
- WB
Lab
Western blot - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - BSA and Azide free (AB271835)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32570).
Blocking/Diluting buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-PDGFR alpha + PDGFR beta antibody [Y92] - C-terminal (<a href='/en-us/products/primary-antibodies/pdgfr-alpha-pdgfr-beta-antibody-y92-c-terminal-ab32570'>ab32570</a>) at 1/1000 dilution
Lane 1:
Western blot - Recombinant human PDGFR beta protein (<a href='/en-us/products/proteins-peptides/recombinant-human-pdgfr-beta-protein-ab60833'>ab60833</a>) at 0.1 µg
Lane 2:
Western blot - Recombinant human PDGFR alpha protein (<a href='/en-us/products/proteins-peptides/recombinant-human-pdgfr-alpha-protein-ab84797'>ab84797</a>) at 0.1 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 1/20000 dilution
false
Exposure time: 3s
Related conjugates and formulations (8)
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Anti-PDGFR alpha + PDGFR beta antibody [Y92] - Low endotoxin, Azide free
-
Anti-PDGFR alpha + PDGFR beta antibody [Y92] - C-terminal
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660 APC
APC Anti-PDGFR alpha + PDGFR beta antibody [Y92] - C-terminal
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421 Alexa Fluor® 405
Alexa Fluor® 405 Anti-PDGFR alpha + PDGFR beta antibody [Y92]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-PDGFR alpha + PDGFR beta antibody [Y92]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-PDGFR alpha + PDGFR beta antibody [Y92]
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HRP Anti-PDGFR alpha + PDGFR beta antibody [Y92]
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578 PE
PE Anti-PDGFR alpha + PDGFR beta antibody [Y92] (C-terminal)
Reactivity data
Product details
ab271835 is the carrier-free version of ab32570.
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
These receptors drive cellular processes like proliferation differentiation and migration. PDGFR alpha and beta operate as a significant part of a receptor complex. They modulate responses in mesenchymal cells and influence developmental pathways. In the vasculature system these receptors play roles in maintaining structure and function of blood vessels. Alterations in receptor activities can affect development of tissues and organs.
Pathways
PDGFR alpha and beta are key players in the PI3K-Akt signaling pathway and MAPK pathway. The activation of these pathways leads to cellular processes like survival and growth. PDGFR activity often interacts with other proteins such as SHP-2 RAS and Akt. These interactions contribute to the regulation of cellular responses to external growth signals embedding PDGFR in a web of intracellular cascade systems.
Product protocols
- Visit the General protocols
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Target data
Additional targets
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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