Anti-HRPT2/Parafibromin antibody [EPR19927] - BSA and Azide free (ab251575)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR19927] to HRPT2/Parafibromin - BSA and Azide free
- Suitable for: Flow Cyt, WB, IHC-P
- Reacts with: Mouse, Rat, Human
Overview
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Product name
Anti-HRPT2/Parafibromin antibody [EPR19927] - BSA and Azide free
See all HRPT2/Parafibromin primary antibodies -
Description
Rabbit monoclonal [EPR19927] to HRPT2/Parafibromin - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: Flow Cyt, WB, IHC-Pmore details -
Species reactivity
Reacts with: Mouse, Rat, Human -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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General notes
ab251575 is the carrier-free version of ab223840 This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
Ab251575 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
This product was previously labelled as HRPT2
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Clonality
Monoclonal -
Clone number
EPR19927 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-HRPT2/Parafibromin antibody [EPR19927] (ab223840) at 1/1000 dilution
Lane 1 : HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Lane 2 : Caco-2 (human colorectal adenocarcinoma cell line) whole cell lysate at 20 µg
Lane 3 : HepG2 (human liver hepatocellular carcinoma cell line) whole cell lysate at 20 µg
Lane 4 : Human fetal kidney lysate at 10 µg
Secondary
Lanes 1-3 : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Lane 4 : Goat Anti-Rabbit IgG Peroxidase Conjugate, specific to the non-reduced form of IgG at 1/10000 dilution
Developed using the ECL technique.
Predicted band size: 61 kDa
Observed band size: 60 kDa why is the actual band size different from the predicted?This data was developed using ab223840, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
Exposure times: Lanes 1-3: 30 seconds; Lane 4: 3 minutes.
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This data was developed using ab223840, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded human kidney (A) and human clear cell renal cell carcinoma (B) labeling HRPT2/Parafibromin with ab223840 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Nuclear staining of human kidney epithelium; human clear cell renal cell carcinoma is negative for HRPT2/Parafibromin (PMID: 23361235). 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. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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This data was developed using ab223840, the same antibody clone in a different buffer formulation.Flow cytometric analysis of 4% paraformaldehyde fixed, 90% methanol permeabilized HeLa (human epithelial cell line from cervix adenocarcinoma) cell line labeling HRPT2/Parafibromin with ab223840 at 1/500 dilution (red) compared with a 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) (ab150077) at 1/2000 dilution was used as the secondary antibody.
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This data was developed using ab223840, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded human parathyroid carcinoma case 1 (A) and human parathyroid carcinoma case 2 (B) labeling HRPT2/Parafibromin with ab223840 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Nuclear staining observed in one parathyroid carcinoma case, while another case was found to be negative for the target (PMID: 16728578). 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. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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This data was developed using ab223840, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded mouse brain tissue labeling HRPT2/Parafibromin with ab223840 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Nuclear staining in neurons in murine neurons is observed. 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. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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This data was developed using ab223840, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded rat brain tissue labeling HRPT2/Parafibromin with ab223840 at 1/1000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Nuclear staining in neurons in rat brain is observed. Counter stained with hematoxylin. Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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