Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Advanced Validation
- Recombinant
- What is this?
5
(1 Review)
|
(1 Publication)
Rabbit Recombinant Monoclonal Myelin PLP antibody. Carrier free. Suitable for ICC/IF, IP, WB, mIHC, IHC-Fr, IHC-P and reacts with Mouse, Rat, Human samples. Cited in 1 publication.
View Alternative Names
PLP, PLP1, Myelin proteolipid protein, Lipophilin
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
Fluorescence multiplex immunohistochemical analysis of the human cerebrum (Formalin/PFA-fixed paraffin-embedded sections). Panel A : merged staining of anti-GFAP (ab68428, gray; Opal™690), anti-Myelin PLP (ab254363, green; Opal™520) and anti-P2Y12 (ab254347, red; Opal™570) on human cerebrum. Panel B : anti-P2Y12 stained on microglial cells. Panel C : anti-Myelin PLP stained on myelin sheaths of oligodendrocytes. Panel D : anti-GFAP stained on astrocytes. Opal Polymer HRP Ms + Rb was used as a secondary antibody. The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. The section was incubated in three rounds of staining : in the order of ab68428 (1/50 dilution), ab254363 (1/2000 dilution), and ab254347 (1/1000 dilution) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins. DAPI (blue) was used as a nuclear counter stain. Image acquisition was performed with Leica SP8 confocal microscope.
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
Fluorescence multiplex immunohistochemical analysis of the human cerebellum (Formalin/PFA-fixed paraffin-embedded sections). Panel A : merged staining of anti-GFAP (ab68428, gray; Opal™690), anti-Myelin PLP (ab254363, green; Opal™520) and anti-P2Y12 (ab254347 red; Opal™570) on human cerebellum. Panel B : anti-P2Y12 stained on microglial cells. Panel C : anti-Myelin PLP stained on myelin sheaths of oligodendrocytes. Panel D : anti-GFAP stained on astrocytes. Opal Polymer HRP Ms + Rb was used as a secondary antibody. The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. The section was incubated in three rounds of staining : in the order of ab68428 (1/50 dilution), ab254363 (1/2000 dilution), and ab254347 (1/1000 dilution) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins. DAPI (blue) was used as a nuclear counter stain. Image acquisition was performed with Leica SP8 confocal microscope.
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling Myelin PLP with ab254363 at 1/2000 (0.261 ug/ml) dilution followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on human cerebrum (PMID : 29081415). Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
Fluorescence multiplex immunohistochemical analysis of human cerebrum tissue (formalin/PFA-fixed paraffin-embedded section). Panel A : merged staining of anti-GFAP (ab68428, gray; Opal™690), anti-Myelin PLP (ab254363, green; Opal™520) and anti-MAP2 (ab254263, red; Opal™570) on human cerebrum tissue. Panel B : anti-MAP2 stained cell body and dendrites of neurons. Panel C : anti-Myelin PLP stained on myelin sheaths of oligodendrocytes. Panel D : anti-GFAP stained on astrocytes. Opal Polymer HRP Ms + Rb was used as a secondary antibody. The immunostaining was performed on a Leica Biosystems BOND®RX instrument with an Opal™ 4-color kit. The section was incubated in three rounds of staining : in the order of ab68428 (1/50 dilution), ab254363 (1/2000 dilution), and ab254263 (1/4000 dilution) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) was used for 20 mins. DAPI (blue) was used as a nuclear counter stain. Image acquisition was performed with Leica SP8 confocal microscope.
The data was developed using ab254363, the same antibody clone in a different buffer formulation.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
Fluorescence multiplex immunohistochemical analysis of human cerebellum tissue (formalin/PFA-fixed paraffin-embedded section). Panel A : merged staining of anti-GFAP (ab68428, gray; Opal™690), anti-Myelin PLP (ab254363, green; Opal™520) and anti-MAP2 (ab254263, red; Opal™570) on human cerebellum tissue. Panel B : anti-MAP2 stained cell body and dendrites of neurons. Panel C : anti-Myelin PLP stained on myelin sheaths of oligodendrocytes. Panel D : anti-GFAP stained on astrocytes. Opal Polymer HRP Ms + Rb was used as a secondary antibody. The immunostaining was performed on a Leica Biosystems BOND®RX instrument with an Opal™ 4-color kit. The section was incubated in three rounds of staining : in the order of ab68428 (1/50 dilution), ab254363 (1/2000 dilution), and ab254263 (1/4000 dilution) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) was used for 20 mins. DAPI (blue) was used as a nuclear counter stain. Image acquisition was performed with Leica SP8 confocal microscope.
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
- IHC-Fr
Unknown
Immunohistochemistry (Frozen sections) - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebellum tissue labeling Myelin PLP with ab254363 at 1/500 (1.042 ug/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on mouse cerebellum. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling Myelin PLP with ab254363 at 1/2000 (0.261 ug/ml) dilution followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on rat cerebrum. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-Fr
Unknown
Immunohistochemistry (Frozen sections) - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebrum tissue labeling Myelin PLP with ab254363 at 1/500 (1.042 ug/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on rat cerebrum. is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-Fr
Unknown
Immunohistochemistry (Frozen sections) - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebrum tissue labeling Myelin PLP with ab254363 at 1/500 (1.042 ug/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on mouse cerebrum. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling Myelin PLP with ab254363 at 1/2000 (0.261 ug/ml) dilution followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on mouse cerebrum (PMID : 28066178). Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
Immunocytochemistry analysis of mouse primary neural/glia cells labelling Myelin PLP with ab254363 at 1/50 dilution. Cells were fixed with 4% paraformaldehyde. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) at 1/1000 was used as the secondary antibody (green). Cells were counterstained with Anti-MAP2 mouse monoclonal antibody (ab11267) at 1/200 dilution and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) (ab150120) at 1/1000 dilution (red). Nuclear DNA was labelled with DAPI (blue).
Confocal image showing cytoplasmic staining in mouse primary glia cells.
Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
Immunocytochemistry analysis of rat primary neural/glia cells labelling Myelin PLP with ab254363 at 1/50 dilution. Cells were fixed with 4% paraformaldehyde. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) at 1/1000 was used as the secondary antibody (green). Cells were counterstained with Anti-Myelin Basic Protein rat monoclonal antibody at 1/100 dilution and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) (ab150120) at 1/1000 dilution (red). Nuclear DNA was labelled with DAPI (blue).
Confocal image showing cytoplasmic staining in rat primary glia cells.
Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection.
- IHC-Fr
Unknown
Immunohistochemistry (Frozen sections) - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebellum tissue labeling Myelin PLP with ab254363 at 1/500 (1.042 ug/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on rat cerebellum. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IP
Unknown
Immunoprecipitation - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Myelin PLP was immunoprecipitated from 0.35 mg Mouse brain tissue lysate with ab254363 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab254363 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse brain tissue lysate 5 ug
Lane 2 : ab254363 IP in Mouse brain tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab254363 in mouse brain tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 6 seconds.
All lanes:
Immunoprecipitation - Anti-Myelin PLP antibody [EPR23504-106] (<a href='/en-us/products/primary-antibodies/myelin-plp-antibody-epr23504-106-ab254363'>ab254363</a>)
Predicted band size: 30 kDa
Observed band size: 20 kDa,23 kDa
false
- WB
Lab
Western blot - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight observed is consistent with what has been described in the literature (PMID : 9247276)
Exposure time : 1 second.
All lanes:
Western blot - Anti-Myelin PLP antibody [EPR23504-106] (<a href='/en-us/products/primary-antibodies/myelin-plp-antibody-epr23504-106-ab254363'>ab254363</a>) at 1/5000 dilution
All lanes:
Human brain tissue lysate at 10 µg
Secondary
All lanes:
VeriBlot for IP secondary antibody(HRP)(<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/1000 dilution
Predicted band size: 30 kDa
Observed band size: 20 kDa,23 kDa
false
- WB
Lab
Western blot - Anti-Myelin PLP antibody [EPR23504-106] - BSA and Azide free (AB275751)
This data was developed using ab254363, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The molecular weight observed is consistent with what has been described in the literature (PMID : 9247276).
Negative control : liver (PMID : 2414013).
Exposure time : 37 seconds.
All lanes:
Western blot - Anti-Myelin PLP antibody [EPR23504-106] (<a href='/en-us/products/primary-antibodies/myelin-plp-antibody-epr23504-106-ab254363'>ab254363</a>) at 1/2000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Mouse liver tissue lysate at 20 µg
Lane 3:
Rat brain tissue lysate at 20 µg
Lane 4:
Rat liver tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 30 kDa
Observed band size: 20 kDa,23 kDa
false
Related conjugates and formulations (6)
-
Anti-Myelin PLP antibody [EPR23504-106]
-
603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-Myelin PLP antibody [EPR23504-106]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-Myelin PLP antibody [EPR23504-106]
-
775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-Myelin PLP antibody [EPR23504-106]
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-Myelin PLP antibody [EPR23504-106]
-
565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-Myelin PLP antibody [EPR23504-106]
Reactivity data
Product details
ab275751 is the carrier-free version of ab254363.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The myelin proteolipid protein contributes to the stability and functionality of the myelin sheath impacting nervous impulse conduction. It plays a structural role in the formation and maintenance of myelin which is essential for rapid signal transmission in the nervous system. PLP can form a complex with DM20 a related isoform which aids in the regulatory processes of myelination. The protein is critical for the compaction and shear resistance of the myelin sheath ensuring efficient neuronal communication.
Pathways
The myelin proteolipid protein is involved in myelination and cell adhesion processes that are part of central nervous system development. It participates in the myelin assembly pathway and interacts with other key proteins like 2'3'-cyclic nucleotide 3'-phosphodiesterase (CNPase) to modulate myelin biogenesis and homeostasis. This interaction is important for the formation and repair of myelin ensuring that signal transduction remains unobstructed in the nervous system.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Cell 187:3120-3140.e29 PubMed38714197
2024
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com