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RecombinantRabMAb

Recombinant Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

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ChIP - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Immunoprecipitation - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Flow Cytometry (Intracellular) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Flow Cytometry (Intracellular) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Immunocytochemistry/ Immunofluorescence - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Immunocytochemistry/ Immunofluorescence - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
  • Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

Key features and details

  • Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
  • Rabbit monoclonal [EPR22506-15] to Rad21 - BSA and Azide free
  • Suitable for: Flow Cyt (Intra), WB, IHC-P, ICC/IF, ChIP, IP
  • Reacts with: Mouse, Rat, Human

Conjugates logo Related conjugates and formulations

APC HRP PE Unconjugated

Overview

  • Product name

    Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free
    See all Rad21 primary antibodies

  • Description

    Rabbit monoclonal [EPR22506-15] to Rad21 - BSA and Azide free

  • Host species

    Rabbit

  • Tested applications

    Suitable for: Flow Cyt (Intra), WB, IHC-P, ICC/IF, ChIP, IPmore details

  • Species reactivity

    Reacts with: Mouse, Rat, Human

  • Immunogen

    Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.

  • Positive control

    • IHC-P: Human breast carcinoma, stomach, mouse stomach and rat colon tissue. ICC/IF: HeLa and NIH/3T3 cells. Flow: HeLa and NIH/3T3 cells. IP: HeLa whole cell lysate.

  • General notes

    ab254483 is the carrier-free version of ab217678.

    Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.

    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.

    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

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab254483 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
Flow Cyt (Intra)
Use at an assay dependent concentration.
WB
Use at an assay dependent concentration. Predicted molecular weight: 72 kDa.
IHC-P
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
ICC/IF
Use at an assay dependent concentration.
ChIP
Use at an assay dependent concentration.
IP
Use at an assay dependent concentration.
Notes
Flow Cyt (Intra)
Use at an assay dependent concentration.
WB
Use at an assay dependent concentration. Predicted molecular weight: 72 kDa.
IHC-P
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
ICC/IF
Use at an assay dependent concentration.
ChIP
Use at an assay dependent concentration.
IP
Use at an assay dependent concentration.

Target

  • Function

    Cleavable component of the cohesin complex, involved in chromosome cohesion during cell cycle, in DNA repair, and in apoptosis. The cohesin complex is required for the cohesion of sister chromatids after DNA replication. The cohesin complex apparently forms a large proteinaceous ring within which sister chromatids can be trapped. At metaphase-anaphase transition, this protein is cleaved by separase/ESPL1 and dissociates from chromatin, allowing sister chromatids to segregate. The cohesin complex may also play a role in spindle pole assembly during mitosis. Also plays a role in apoptosis, via its cleavage by caspase-3/CASP3 or caspase-7/CASP7 during early steps of apoptosis: the C-terminal 64 kDa cleavage product may act as a nuclear signal to initiate cytoplasmic events involved in the apoptotic pathway.

  • Sequence similarities

    Belongs to the rad21 family.

  • Domain

    The C-terminal part associates with the head of SMC1A, while the N-terminal part binds to the head of SMC3.

  • Post-translational
    modifications

    Cleaved by separase/ESPL1 at the onset of anaphase. Cleaved by caspase-3 and caspase-7 at the beginning of apoptosis. The cleavage by ESPL1 and caspase-3 take place at different sites.
    Phosphorylated; becomes hyperphosphorylated in M phase of cell cycle. The large dissociation of cohesin from chromosome arms during prophase may be partly due to its phosphorylation by PLK.

  • Cellular localization

    Nucleus. Chromosome. Chromosome > centromere. Associates with chromatin. Before prophase it is scattered along chromosome arms. During prophase, most of cohesin complexes dissociate from chromatin probably because of phosphorylation by PLK, except at centromeres, where cohesin complexes remain. At anaphase, it is cleaved by separase/ESPL1, leading to the dissociation of the complex from chromosomes, allowing chromosome separation. Once cleaved by caspase-3, the C-terminal 64 kDa cleavage product translocates to the cytoplasm, where it may trigger apoptosis.
  • Information by UniProt

  • Database links

    • Alternative names

      • CDLS4 antibody
      • Double-strand-break repair protein rad21 homolog antibody
      • hHR21 antibody
      • HR21 antibody
      • HRAD21 antibody
      • KIAA0078 antibody
      • MCD1 antibody
      • Nuclear matrix protein 1 antibody
      • NXP-1 antibody
      • NXP1 antibody
      • Protein involved in DNA double-strand break repair antibody
      • RAD21 antibody
      • RAD21 homolog (S. pombe) antibody
      • RAD21 homolog antibody
      • RAD21_HUMAN antibody
      • Scc1 antibody
      • SCC1 homolog antibody
      see all

    Images

    • ChIP - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      ChIP - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Chromatin was prepared from MCF7 cells according to the Abcam X-ChIP protocol. Cells were fixed with formaldehyde for 10min.


      The ChIP was performed with 25 µg of chromatin, 5 µg of ab217678 (red), and 20 µl of Protein A/G sepharose beads. 5 μg of rabbit normal IgG was added to the beads control (gray). The immunoprecipitated DNA was quantified by real time PCR (sybr green approach).


      Primers and probes are located in the first kb of the transcribed region.


      The observed enrichment profile of Rad21 binding is consistent with what has been described in the literature (PMID: 23145106)


       

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).
    • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Immunohistochemical analysis of paraffin-embedded rat colon tissue labeling Rad21 using ab217678 at 1/1000 dilution for 30 minutes at room temperature, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining on rat colon (PMID: 25575569) is observed. Counterstained with Hematoxylin. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.

       

      Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is  a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).

      Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

    • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Immunohistochemical analysis of paraffin-embedded mouse stomach tissue labeling Rad21 using ab217678 at 1/1000 dilution for 30 minutes at room temperature, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining on mouse stomach (PMID: 25575569) is observed. Counterstained with Hematoxylin. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.

       

      Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is  a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).

      Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

    • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Immunohistochemical analysis of paraffin-embedded human stomach tissue labeling Rad21 using ab217678 at 1/1000 dilution for 30 minutes at room temperature, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining on human stomach (PMID: 25575569) is observed. Counterstained with Hematoxylin. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.

       

      Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is  a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).

       

       

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).

      Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

    • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue labeling Rad21 using ab217678 at 1/1000 dilution for 30 minutes at room temperature, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Nuclear staining on the human breast carcinoma (PMID: 21255398) is observed. Counterstained with Hematoxylin. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.

       

      Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is  a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).

       

       

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).

      Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

    • Immunoprecipitation - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Immunoprecipitation - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Rad21 was immunoprecipitated from 0.35mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate with ab217678 at 1/30 dilution. Western blot was performed on the immunoprecipitate using ab217678 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (ab131366) was used as the secondary antibody at 1/5000 dilution.


      Lane 1: HeLa whole cell lysate 10µg (input)
      Lane 2: ab217678 IP in HeLa whole cell lysate.
      Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab217678 in HeLa whole cell lysate.


      Blocking and dilution buffer and concentration: 5% NFDM/TBST.


      Exposure time: 3 seconds.


      Faint band below 75kDa in lane 2 could be Rad21 cleavage product as described in the literature (PMID: 28854249).

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).
    • Flow Cytometry (Intracellular) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Flow Cytometry (Intracellular) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed NIH/3T3 (mouse embryonic fibroblast) cell line labeling Rad21 using ab217678 at 1/500 dilution (red) compared with a Rabbit monoclonal IgG (ab172730, Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody. 

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).

       

    • Flow Cytometry (Intracellular) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Flow Cytometry (Intracellular) - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed HeLa (human cervix adenocarcinoma epithelial cell) cell line labeling Rad21 using ab217678 at 1/500 dilution (red) compared with a Rabbit monoclonal IgG (ab172730, Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody. 

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).

       

    • Immunocytochemistry/ Immunofluorescence - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Immunocytochemistry/ Immunofluorescence - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labeling Rad21 with ab217678 at 1/100 dilution, followed by an AlexaFluor®488 Goat anti-Rabbit secondary antibody (ab150077) at 1/1000 dilution (green). Confocal image showing nuclear staining in NIH/3T3 cell line is observed. The nuvlear counterstain is DAPI (Blue). Tubulin is counterstained using Ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at 1/200 dilution.


      Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is an AlexaFluor®488 Goat anti-Rabbit secondary (ab150077) at 1/1000 dilution.


       

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).
    • Immunocytochemistry/ Immunofluorescence - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Immunocytochemistry/ Immunofluorescence - Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

      Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells labeling Rad21 with ab217678 at 1/100 dilution, followed by an AlexaFluor®488 Goat anti-Rabbit secondary antibody (ab150077) at 1/1000 dilution (green). Confocal image showing nuclear staining in HeLa cell line is observed. The nuvlear counterstain is DAPI (Blue). Tubulin is counterstained using Ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at 1/200 dilution.


      Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is an AlexaFluor®488 Goat anti-Rabbit secondary (ab150077) at 1/1000 dilution.


       

      This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab217678).
    • Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)
      Anti-Rad21 antibody [EPR22506-15] - BSA and Azide free (ab254483)

    Protocols

    To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

    Click here to view the general protocols

    References (0)

    Publishing research using ab254483? Please let us know so that we can cite the reference in this datasheet.

    ab254483 has not yet been referenced specifically in any publications.

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