Overview

  • Product name
    Anti-PLVAP / PV-1 antibody [MECA-32]
    See all PLVAP / PV-1 primary antibodies
  • Description
    Rat monoclonal [MECA-32] to PLVAP / PV-1
  • Host species
    Rat
  • Specificity
    This antibody is specific to PLVAP / PV-1.
  • Tested applications
    Suitable for: Flow Cyt, IP, IHC-Fr, ICC, WBmore details
  • Species reactivity
    Reacts with: Mouse
  • Immunogen

    Tissue, cells or virus corresponding to Mouse PLVAP/ PV-1.

  • Positive control
    • Embryonic and adult mouse endothelial cell surfaces with the exceptions of cardiac, skeletal muscle and brain.
  • General notes

    Previously labelled as PLVAP.

Properties

Applications

Our Abpromise guarantee covers the use of ab27853 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
Flow Cyt Use 1µg for 106 cells.

ab18450 - Rat monoclonal IgG2a, is suitable for use as an isotype control with this antibody.

 

IP Use at an assay dependent concentration.
IHC-Fr Use at an assay dependent concentration.

Acetone fixed sections.

ICC Use at an assay dependent concentration.
WB Use at an assay dependent concentration. Detects a band of approximately 50 - 55 kDa (predicted molecular weight: 51 kDa).

Target

  • Function
    Involved in the formation of stomatal and fenestral diaphragms of caveolae. May function in microvascular permeability.
  • Tissue specificity
    Expressed in lung, kidney, heart, aorta, placenta, muscle, pituitary gland, adrenals, mammary gland, bladder, lymph node, bone marrow, trachea, digestive tract, liver and tumor-associated endothelium.
  • Cellular localization
    Cell membrane. Membrane > caveola. Cytoplasm > perinuclear region. Membrane-associated protein of caveolae. Found in fenestral and stomatal diaphragms in fenestrated endothelia and transendothelial channels. Also colocalized with CAV1 in perinuclear region.
  • Information by UniProt
  • Database links
  • Alternative names
    • FELS antibody
    • Fenestrated endothelial linked structure protein antibody
    • Fenestrated endothelial-linked structure protein antibody
    • gp68 antibody
    • Hypothetical protein DKFZp667O074 antibody
    • Meca 32 antigen antibody
    • MECA32 antigen antibody
    • Panendothelial cell antigen antibody
    • Plasmalemma vesicle associated protein antibody
    • Plasmalemma vesicle protein 1 antibody
    • Plasmalemma vesicle-associated protein antibody
    • Plvap antibody
    • PLVAP_HUMAN antibody
    • PV 1 antibody
    • PV-1 antibody
    • PV1 antibody
    • PV1 protein antibody
    see all

References

This product has been referenced in:
  • Englinger B  et al. Intrinsic fluorescence of the clinically approved multikinase inhibitor nintedanib reveals lysosomal sequestration as resistance mechanism in FGFR-driven lung cancer. J Exp Clin Cancer Res 36:122 (2017). Read more (PubMed: 28882160) »
  • Wang XL  et al. VEGFR-3 blocking deteriorates inflammation with impaired lymphatic function and different changes in lymphatic vessels in acute and chronic colitis. Am J Transl Res 8:827-41 (2016). IHC-Fr ; Mouse . Read more (PubMed: 27158372) »
See all 7 Publications for this product

Customer reviews and Q&As

1-3 of 3 Abreviews or Q&A

Answer

Thank you for your patience.

For ab27853, it is as I had thought in my last email.The application was added based on publications showing that [MECA-32] has worked in IHC-Fr, e.g.

"The Adnectin CT-322 is a novel VEGF receptor 2 inhibitor that decreases tumor burden in an orthotopic mouse model of pancreatic cancer" by Dineen et al., BMC Cancer 2008, 8:352 (see attachment).

I hope this information is helpful to you. Please do not hesitate to contact us if you need any more advice or information.

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Answer

Thank you for confirming these details and for your cooperation. The details provided enable us to closely monitor the quality of our products.

I am sorry the product ab2350 did not perform as stated on the datasheet and for the inconvenience this has caused. As requested, I have issued a free of charge replacement with the order number xxx with ab27853.

To check the status of the order please contact our Customer Service team and reference this number.

Please note that this free of charge replacement vial is also covered by our Abpromise guarantee. Should you still be experiencing difficulties, or if you have any further questions, please do not hesitate to let us know.

As for the IHC-Fr protocols:


For ab27853, I will need to check with the supplying lab if they have any details on that. As far as I know, it was reported to them by other researchers that the antibody works in IHC-Fr. I will let you know what I find out.

I have attached our IHC-Fr protocols to help you further in the meantime.


For ab53444,we have the following protocol on file:

Indirect Immunostaining of Frozen Tissue Sections

For use with unconjugated monoclonal and polyclonal antibodies.
Please note that a certain level of technical skill and immunological knowledge is required for the successful design and implementation of these techniques - these are guidelines only and may need to be adjusted for particular applications.
Reagents
1. 0.3% H2O2‎, 70% methanol in TBS
1 ml of 30% H2O2‎ per 100 ml methanol/TBS.
2. TBS stock solution (10x)
NaCl, 87.66 g
Tris base, 60.55 g
Distilled water, 1 liter
Adjust pH to 7.4 using concentrated HCl.
Method
In most cases, we recommend that tissues are snap-frozen in liquid nitrogen, then prepared as 4-6 μm sections using a cryostat.
Allow sections to air dry for at least 1 hour.
Fix sections in dry acetone for 15 minutes. Allow to evaporate for 10 minutes.
Block endogenous peroxidase (if necessary) by immersing slides in 0.3% H2O2‎ in 70% methanol/TBS for 30 minutes. Wash once in TBS.
Incubate sections for 10 minutes in 10% normal serum from the species in which the secondary was raised. Tap excess serum off the slides before staining.
Incubate sections with primary antibody for at least 30 minutes at room temperature in a humid chamber, or overnight at 4°C. Wash 3 times in TBS.
Add enzyme-conjugated secondary antibody at the recommended dilution (see specific datasheet for details). Incubate for at least 30 minutes at room temperature. Wash 3 times in TBS.
Incubate with the appropriate substrate solution for the recommended period of time (it is suggested to useDAB substrate with HRP-conjugated antibodies, and Fast Red/Napthol AS-MX for Alkaline Phosphatase-conjugated antibodies). Wash once in water.
Counterstain with hematoxylin for 1-10 minutes. “Blue” with running water for 5 minutes. Then wash.
Mount in aqueous mounting medium, or alternatively dehydrate through a graded series of alcohols and xylene/solvent, and mount in synthetic mountant.

Notes
- Do not allow slides to dry out after the fixation step, as drying will result in damage to the tissue structure.
- Beware, certain substrates are soluble in alcohol – please refer to manufacturer's information for details.
- Appropriate controls should always be carried out. It may be useful to include a sample in which no primary antibody is used at all, in order to determine any non-specific binding of the secondary reagent to the target tissue.

In addition, you can also check the Abreviews section where 7 IHC-Fr reviews had been submitted by other customers:
https://www.abcam.com/CD68-antibody-FA-11-ab53444-reviews.html




I wish you the best of luck with your research.

Please let me know if there is anything else I can do for you.

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Answer

Thank you for contacting us. While I am unaware of any references describingACVRL1 expression in tumors, the human protein atlas (linked below) does show that "distinct cytoplasmic staining with a granular pattern was observed in thyroid cancers, malignant lymphomas and in a few malignant melanomas, colorectal, gastric, pancreatic and renal cancers. Malignant cells in general were negative." http://www.proteinatlas.org/ENSG00000139567/cancer Additionally, because ACVRL1 is88%homologous betweenmouse and human, it will be difficult to find an antibody to that target which will react with mouse and not human epithelial cells. If you are looking to specifically detect mouse endothelial cells, you may be interested in the PLVAP antibody clone MECA-32 (ab27853), which is described in http://www.ncbi.nlm.nih.gov/pubmed/7626790?dopt=AbstractPlus. I hope this helps, please let me know if you need any additional information.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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