Adult mouse DRG was fixed in 4% paraformaldehyde, cryostat-sectioned, and then stained for PAP immunoreactivity (1:500 dilution), showing immunoreactive material in primary sensory neurons.  Photomicrograph by Dr. Mark Zilka, Univ. of North Carolina.

Adult mouse DRG was fixed in 4% paraformaldehyde, cryostat-sectioned, and then stained for PAP immunoreactivity (1:500 dilution), showing immunoreactive material in primary sensory neurons. Photomicrograph by Dr. Mark Zilka, Univ. of North Carolina.

Adult mouse spinal cord was fixed in 4% paraformaldehyde, paraffin-embedded and sectioned, and then sections were stained for PAP immunoreactivity (1:500 dilution).  Adjacent sections were co-stained for !B4 and Calcitonin Gene-Related Protein (CGRP) (other sensory neuronal markers).  Photomicrograph by Dr. Mark Zilka, University of North Carolina.

Adult mouse spinal cord was fixed in 4% paraformaldehyde, paraffin-embedded and sectioned, and then sections were stained for PAP immunoreactivity (1:500 dilution). Adjacent sections were co-stained for !B4 and Calcitonin Gene-Related Protein (CGRP) (other sensory neuronal markers). Photomicrograph by Dr. Mark Zilka, University of North Carolina.

Adult mouse spinal cord was fixed in 4% paraformaldehyde, paraffin-embedded and sectioned, and then sections were stained for PAP immunoreactivity (1:500 dilution).  Immunoreactivity shown in Rexed Lamina 2 of the dorsal horn gray matter of the spinal cord.  Photomicrograph by Dr. Mark Zilka, University of North Carolina.

Adult mouse spinal cord was fixed in 4% paraformaldehyde, paraffin-embedded and sectioned, and then sections were stained for PAP immunoreactivity (1:500 dilution). Immunoreactivity shown in Rexed Lamina 2 of the dorsal horn gray matter of the spinal cord. Photomicrograph by Dr. Mark Zilka, University of North Carolina.

Anti-Prostatic Acid Phosphatase (PAP)

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Details

Chickens were immunized with recombinant mouse Prostatic Acid Phosphatase protein. After repeated injections, immune eggs were collected from laying hens, from which IgY antibody were prepared ("anti-PAP IgY fraction"). Some of this antibody was further purified using an agarose matrix to which the PAP protein was covalently attached ("Affinity-purified anti-PAP"). The final preparation in the accompanying vial contains 10 mg/mL of the "anti-PAP IgY fraction" supplemented with 20 µg/mL of the "affinity-purified anti-PAP" plus 50% (v/v) glycerol (to prevent freezing at –20˚C). Finally, this antibody preparation was filter-sterilized (0.45 mm) and 200 ul aliquots prepared.

Volume: 200 µL

Concentration: 10 mg/mL

Clonality: Polyclonal

Host Species: Chicken

Species Reactivity: Human, Mouse, Rat

Applications: IHC, WB

Protein Name / Synonyms: Prostatic acid phosphatase (PAP) (EC 3.1.3.2) (5'-nucleotidase) (5'-NT) (EC 3.1.3.5) (Ecto-5'-nucleotidase) (Thiamine monophosphatase) (TMPase) [Cleaved into: PAPf39]

Gene ID: ACPP

Antibody Registry ID (RRID): AB_2313557

Physical State: Liquid

Validation and Application Notes

Expected Banding Pattern: 45 kDa

Western Blot Dilution Range: 1:1000-1:2000

IHC Dilution Range: 1:500-1:1000

Quality Control

Antibodies were analyzed using immunohistochemistry with tissue sections through a 10%-formalin fixed adult mouse. Sections were examined for PAPpositive dorsal root ganglion sensory neurons. Secondary antibodies (fluorescein-labeled goat anti-chicken IgY, Aves Cat. #F-1004) were used at a concentration of 1:500.

Storage

Store at -20°C in the dark. Under these conditions, the antibodies should have a shelf life of at least 2 years (provided they remain sterile). For longer storage periods, store at -80°C. Note that storage at this lower temperature will destroy some antibody activity due to water crystallization.

NOTE

Aves Labs products are intended for use as research laboratory reagents. They are not intended for use as diagnostic or therapeutic reagents in humans.


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Citations


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