Anti-Cathepsin D 抗体 [EPR3056Y] - BSA and Azide free
Anti-Cathepsin D antibody [EPR3056Y] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- 詳細を見る
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(1 Publication)
Rabbit Recombinant Monoclonal Cathepsin D antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB, Flow Cyt (Intra) and reacts with Human samples. Cited in 1 publication.
別名を表示する
CPSD, CTSD, Cathepsin D
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-Cathepsin D antibody [EPR3056Y] - BSA and Azide free (AB207550)
This data was developed using ab75811, the same antibody clone in a different buffer formulation. Intracellular Flow Cytometry analysis of MCF7 (Human breast adenocarcinoma epithelial cell) cells labeling Cathepsin D with purified ab75811 at 1/20 dilution (10 μg/mL) (Red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) secondary antibody was used at 1/2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Cathepsin D antibody [EPR3056Y] - BSA and Azide free (AB207550)
This data was developed using ab75811, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of MCF7 (Human breast adenocarcinoma epithelial cell) cells labeling Cathepsin D with purified ab75811 at 1/50 dilution (1.88 µg/mL). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1/200 (2.5 µg/mL). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1/1000 (2 µg/mL) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cathepsin D antibody [EPR3056Y] - BSA and Azide free (AB207550)
This data was developed using ab75811, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human thyroid cancer tissue sections labeling Cathepsin D with purified ab75811 at 1/100 dilution (0.94 µg/mL). Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 1 (pH 6.0). Rabbit specific IHC polymer detection kit HRP/DAB (ab209101) was used as the secondary antibody. Negative control : PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
- WB
Unknown
Western blot - Anti-Cathepsin D antibody [EPR3056Y] - BSA and Azide free (AB207550)
This data was developed using ab75811, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-Cathepsin D antibody [EPR3056Y] (<a href='/products/primary-antibodies/cathepsin-d-antibody-epr3056y-ab75811'>ab75811</a>) at 1/1000 dilution
All lanes:
MCF7 (Human breast adenocarcinoma epithelial cell) whole cell lysate at 15 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/20000 dilution
Predicted band size: 44 kDa
Observed band size: 14 kDa,44 kDa
false
- WB
Lab
Western blot - Anti-Cathepsin D antibody [EPR3056Y] - BSA and Azide free (AB207550)
Lanes 1 - 4 : Merged signal (red and green). Green - ab75811 observed at 44 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab75811 was shown to specifically react with in wild-type A431 cells as signal was lost in CTSD knockout cells. Wild-type and CTSD knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% NF Milk. ab75811 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20000 dilution respectively. Blots were developed 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 1/20000 dilution for 1 hour at room temperature before imaging.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab75811).
All lanes:
Western blot - Anti-Cathepsin D antibody [EPR3056Y] (<a href='/products/primary-antibodies/cathepsin-d-antibody-epr3056y-ab75811'>ab75811</a>) at 1/1000 dilution
Lane 1:
Wild-type A-431 (Human epidermoid carcinoma cell line) whole cell lysate at 40 µg
Lane 2:
CTSD knockout A-431 (Human epidermoid carcinoma cell line) whole cell lysate at 40 µg
Lane 2:
Western blot - Human CTSD knockout A-431 cell line (<a href='/products/cell-lines/human-ctsd-knockout-a-431-cell-line-ab261891'>ab261891</a>)
Lane 3:
Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 40 µg
Lane 4:
MCF7 (Human breast adenocarcinoma cell line) whole cell lysate at 40 µg
Predicted band size: 44 kDa
Observed band size: 44 kDa
false
関連する標識済み抗体及び組成の異なる製品 (1)
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Anti-Cathepsin D antibody [EPR3056Y]
Reactivity data
製品の詳細
ab207550 is the carrier-free version of ab75811.
Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.
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.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存期間
短期保存温度
長期保存温度
分注に関する情報
保管に関する情報
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The enzymatic activity of Cathepsin D is important for cellular maintenance and apoptosis. This protease does not act within larger protein complexes but contributes to the degradation of extracellular and intracellular proteins. It mediates processes like antigen processing where it deconstructs proteins into peptides that are presented on major histocompatibility complex (MHC) molecules. ELISA tests can quantify its expression levels sometimes termed as CTSD activity in various biological samples offering insights into its role within cellular environments.
Pathways
Cathepsin D involvement includes the lysosomal degradation pathway and the apoptotic signaling pathway. In the lysosomal degradation pathway Cathepsin D breaks down proteins and peptides a process important for cellular recycling and energy release. It interacts with other lysosomal enzymes such as Cathepsin B in this pathway ensuring comprehensive breakdown of cellular waste. The apoptotic signaling pathway involves the regulation of programmed cell death where Cathepsin D can influence the activation of downstream proteins like Bcl-2 and Bax which control cell survival.
製品プロトコール
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ターゲットの情報
文献 (1)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 12:4643 PubMed34330919
2021
Applications
Unspecified application
Species
Unspecified reactive species
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