Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal ADRM1/ARM-1 antibody. Carrier free. Suitable for IHC-P, IP, Flow Cyt, WB, ICC/IF and reacts with Human samples.
View Alternative Names
GP110, ADRM1, Proteasomal ubiquitin receptor ADRM1, 110 kDa cell membrane glycoprotein, Adhesion-regulating molecule 1, Proteasome regulatory particle non-ATPase 13, Rpn13 homolog, Gp110, ARM-1, hRpn13
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
This data was developed using ab157185, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human gastric cancer tissue sections labeling ADRM1/ARM-1 with Purified ab157185 at 1 : 9000 (0.07 μg/ml). Heat mediated antigen retrieval was performed using Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) . Tissue was counterstained with Hematoxylin. Rabbit specific IHC polymer detection kit HRP/DAB (ab209101) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
This data was developed using ab157185, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human liver tissue sections labeling ADRM1/ARM-1 with Purified ab157185 at 1 : 9000 (0.07 μg/ml). Heat mediated antigen retrieval was performed using Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) . Tissue was counterstained with Hematoxylin. Rabbit specific IHC polymer detection kit HRP/DAB (ab209101) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
This data was developed using ab249293, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of K-562 (Human chronic myelogenous leukemia lymphoblast) cells labeling ADRM1/ARM-1 with Purified ab249293 at 1 : 1000 dilution (0.6 μg/ml). Cells were fixed in 100% Methanol and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A]+H21 : L21 - 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.
- Flow Cyt
Lab
Flow Cytometry - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
This data was developed using ab249293, the same antibody clone in a different buffer formulation.
Flow Cytometry analysis of K-562 (Human chronic myelogenous leukemia lymphoblast) cells labelling ADRM1/ARM-1 with Purified ab249293 at 1 : 60 dilution (10 μg/ml) (Red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor® 488, ab150081) secondary antibody was used at 1 : 2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabelled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- IP
Lab
Immunoprecipitation - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
This data was developed using ab157185, the same antibody clone in a different buffer formulation.ADRM1/ARM-1 was immunoprecipitated from 0.35 mg Raji (Human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 µg with ab157185 at 1/100 dilution (2µg). VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Raji (Human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 µg
Lane 2 : abab157185 IP in Raji whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab157185 in Raji whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] (<a href='/en-us/products/primary-antibodies/adrm1-arm-1-antibody-epr11449b-ab157185'>ab157185</a>)
Predicted band size: 42 kDa
Observed band size: 42 kDa
false
- WB
Lab
Western blot - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
This data was developed using ab157185, the same antibody clone in a different buffer formulation.
Lanes 1-4 : Merged signal (red and green). Green - ab157185 observed at 42 kDa. Red - loading control ab8245 observed at 36 kDa.
ab157185 Anti-ADRM1/ARM-1 antibody [EPR11449(B)] was shown to specifically react with ADRM1/ARM-1 in wild-type HEK293T cells. Loss of signal was observed when knockout cell line ab266765 (knockout cell lysate ab257816) was used. Wild-type and ADRM1/ARM-1 knockout samples were subjected to SDS-PAGE. ab157185 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] (<a href='/en-us/products/primary-antibodies/adrm1-arm-1-antibody-epr11449b-ab157185'>ab157185</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK293T cell lysate at 20 µg
Lane 2:
ADRM1 knockout HEK293T cell lysate at 20 µg
Lane 2:
Western blot - Human ADRM1 (ARM-1) knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-adrm1-arm-1-knockout-hek-293t-cell-line-ab266765'>ab266765</a>)
Lane 3:
K-562 cell lysate at 20 µg
Lane 4:
Raji cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/10000 dilution
Predicted band size: 42 kDa
Observed band size: 42 kDa
false
- WB
Unknown
Western blot - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
All lanes:
Western blot - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] (<a href='/en-us/products/primary-antibodies/adrm1-arm-1-antibody-epr11449b-ab157185'>ab157185</a>) at 1/1000 dilution
All lanes:
Raji (Human Burkitt's lymphoma B lymphocyte) whole cell lysate
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 42 kDa
false
- WB
Unknown
Western blot - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] - BSA and Azide free (AB249293)
All lanes:
Western blot - Anti-ADRM1/ARM-1 antibody [EPR11449(B)] (<a href='/en-us/products/primary-antibodies/adrm1-arm-1-antibody-epr11449b-ab157185'>ab157185</a>) at 1/10000 dilution
Lane 1:
Ramos (Human Burkitt's lymphoma B lymphocyte) whole cell lysate at 15 µg
Lane 2:
HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate at 15 µg
Lane 3:
K-562 (Human chronic myelogenous leukemia lymphoblast) whole cell lysate at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 42 kDa
false
Related conjugates and formulations (6)
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Anti-ADRM1/ARM-1 antibody [EPR11449(B)]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-ADRM1/ARM-1 antibody [EPR11449(B)]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-ADRM1/ARM-1 antibody [EPR11449(B)]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-ADRM1/ARM-1 antibody [EPR11449(B)]
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660 APC
APC Anti-ADRM1/ARM-1 antibody [EPR11449(B)]
-
775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-ADRM1/ARM-1 antibody [EPR11449(B)]
Reactivity data
Product details
ab249293 is the carrier-free version of ab157185.
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
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The ADRM1/ARM-1 protein binds ubiquitinated substrates and shuttles them to the 26S proteasome for degradation. It acts as a receptor on the regulatory particle of the proteasome complex where it recruits deubiquitinating enzymes. This positions ADRM1 as an integral part of the protein degradation machinery ensuring removal of damaged misfolded or unnecessary proteins and maintaining cellular protein homeostasis.
Pathways
ADRM1 plays a significant role within the ubiquitin-proteasome pathway which is important for protein catabolism. It partners with regulatory proteins like Rpn13 to mediate the recognition and processing of polyubiquitinated substrates. The efficient functioning of this pathway highlights its importance in regulating the cell cycle and various signaling pathways including NF-kB signaling which affects immune response and apoptosis.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
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