Anti-PARP1 antibody [Y17] - BSA and Azide free
- RabMAb
- KO Validated
- 각 태그의 뜻
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Knockout Tested Rabbit Monoclonal PARP1 antibody. Carrier free. Suitable for ICC/IF, Flow Cyt, WB and reacts with Human samples.
대체 명칭 보기
ADPRT, PPOL, PARP1, Poly [ADP-ribose] polymerase 1, PARP-1, ADP-ribosyltransferase diphtheria toxin-like 1, DNA ADP-ribosyltransferase PARP1, NAD(+) ADP-ribosyltransferase 1, Poly[ADP-ribose] synthase 1, Protein poly-ADP-ribosyltransferase PARP1, ARTD1, ADPRT 1
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-PARP1 antibody [Y17] - BSA and Azide free (AB284670)
This data was developed using ab32378, the same antibody clone in a different buffer formulation.
HEK293T wild-type and PARP1 knockout cells (ab266598) were labelled with a green or violet, fluorescent dye, respectively. Wild-type and knockout cells were mixed in a 1 : 1 ratio, fixed in 4% PFA and permeabilized in 0.1% Triton X-100.
Antibody staining was quantified using the Attune NxT Flow Cytometer with representative images showing the staining intensity in the knockout population (pink histogram, dashed line) compared to the wild-type cells (green histogram, solid line). Histograms with dotted lines represent secondary antibody-only controls in both wild-type and knockout cells.
Antibody dilution : 0.5 μg/μL.
This data was provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-PARP1 antibody [Y17] - BSA and Azide free (AB284670)
This data was developed using ab32378, the same antibody clone in a different buffer formulation.
ab32378 was shown to react with PARP1 in wild-type HEK293T cells in immunocytochemistry with loss of signal observed in PARP1 knockout cell line ab266598. Wild-type and knockout cells were mixed and pelleted at a 1 : 1 ratio on coverslips. The cells were fixed with 4% paraformaldehyde (15 min) then permeabilized with 0.1% Triton X-100 (10min) and then blocked with 1x PBS, 0.01% Triton X-100, 5% BSA, 5% NGS. The cells were then incubated with ab32378 at 1/500 dilution overnight at 4°C followed by a further incubation at room temperature for 1h with a goat anti-rabbit secondary antibody to (Alexa Fluor® 555) at 0.5 μg/ml. Acquisition of the green (wild-type), red (antibody staining) and far-red (knockout) channels was performed. Representative grayscale images of the red channel are shown. Wild-type and knockout cells are outlined with yellow and magenta dashed line, respectively. Schematic representation of the mosaic strategy used is shown on the bottom-right panel. Image was acquired with a Zeiss (LSM-880).
This data was provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.
- IP
Supplier Data
Immunoprecipitation - Anti-PARP1 antibody [Y17] - BSA and Azide free (AB284670)
This data was developed using ab32378, the same antibody clone in a different buffer formulation.
Immunoprecipitation of PARP1 in HEK293T cells. Lysates were prepared and immunoprecipitation was performed using 3.8 μg of ab32378 pre-coupled to Protein A beads. Samples were then washed and processed for western blot.
This data was provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.
All lanes:
Immunoprecipitation - Anti-PARP1 antibody [Y17] (<a href='/ko/products/primary-antibodies/parp1-antibody-y17-ab32378'>ab32378</a>) at 3.8 µg
All lanes:
HEK293T cell lysates
Predicted band size: 113 kDa
false
- WB
Supplier Data
Western blot - Anti-PARP1 antibody [Y17] - BSA and Azide free (AB284670)
This data was developed using ab32378, the same antibody clone in a different buffer formulation.
ab32378 was shown to react with PARP1 in wild-type HEK293T cells in Western blot with loss of signal observed in PARP1 knockout cell line ab266598. Wild-type HEK293T and PARP1 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 5% milk in TBST for 1 hr before incubation with ab32378 overnight at 4 °C at a 1/1000 dilution. Blots were incubated with secondary antibodies at 0.2 µg/mL before imaging.
This data was provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.
All lanes:
Western blot - Anti-PARP1 antibody [Y17] (<a href='/ko/products/primary-antibodies/parp1-antibody-y17-ab32378'>ab32378</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK293T lysate at 30 µg
Lane 2:
PARP1 knock-out HEK293T lysate at 30 µg
Lane 2:
Western blot - Human PARP1 knockout HEK-293T cell line (<a href='/ko/products/cell-lines/human-parp1-knockout-hek-293t-cell-line-ab266598'>ab266598</a>)
Predicted band size: 113 kDa
false
- WB
Unknown
Western blot - Anti-PARP1 antibody [Y17] - BSA and Azide free (AB284670)
This data was developed using ab32378, the same antibody clone in a different buffer formulation.
Lane 1:
Jurkat cell lysate.
Lane 2:
Jurkat and Camptothecin cell lysate.
false
- WB
Lab
Western blot - Anti-PARP1 antibody [Y17] - BSA and Azide free (AB284670)
This data was developed using the hybridoma version of ab32378, the same antibody clone in a different buffer formulation.
Lane 1 : Wild type HAP1 whole cell lysate (20 μg)
Lane 2 : PARP1 knockout HAP1 whole cell lysate (20 μg)
Lane 3 : HeLa whole cell lysate (20 μg)
Lane 4 : MCF7 whole cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab32378 observed at 125 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab32378 was shown to specifically react with PARP1 when PARP1 knockout samples were used. Wild-type and PARP1 knockout samples were subjected to SDS-PAGE. ab32378 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/10000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) ab216773 and 680CW Goat anti Mouse secondary antibodies at 1/10000 dilution for 1 hour at room temperature before imaging.
Produced using the hybridoma version.
All lanes:
Western blot - Anti-PARP1 antibody [Y17] (<a href='/ko/products/primary-antibodies/parp1-antibody-y17-ab32378'>ab32378</a>)
Predicted band size: 113 kDa
false
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-PARP1 antibody [Y17]
Reactivity 정보
제품 세부 정보
ab284670 is the carrier-free version of ab32378
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.
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.
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추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Poly(ADP-ribose) polymerase 1 functions to maintain genomic stability by acting within the base excision repair complex. This complex is important for the detection and repair of DNA damage preventing the accumulation of mutations. By acting at sites of DNA stress PARP1 facilitates the binding of DNA repair proteins stabilizing the DNA structure during the repair process. This role is significant for cells that undergo frequent DNA replication or are exposed to high levels of genotoxic stress.
Pathways
The PARP1 protein is integral to the DNA damage response and repair pathway. It interacts with other proteins such as XRCC1 to coordinate repair activities at damaged DNA sites. Another important pathway involving PARP1 is the apoptosis pathway where excessive activation of PARP1 can lead to cell death due to depletion of cellular NAD+ and ATP. This indicates its dual role in both promoting cell survival through DNA repair and contributing to cell death when damage is irreparable.
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타겟 정보
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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