Astana Biomed Group, an authorized Abcam distributor in Central Asia

Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)

Key features and details

  • Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
  • Rabbit monoclonal [EPR16866] to Cellubrevin - BSA and Azide free
  • Suitable for: Flow Cyt, ICC, WB, IP
  • Reacts with: Human

Overview

  • Product name

    Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free
    See all Cellubrevin primary antibodies

  • Description

    Rabbit monoclonal [EPR16866] to Cellubrevin - BSA and Azide free

  • Host species

    Rabbit

  • Tested applications

    Suitable for: Flow Cyt, ICC, WB, IPmore details

  • Species reactivity

    Reacts with: Human

  • Immunogen

    Recombinant full length protein. This information is proprietary to Abcam and/or its suppliers.

  • General notes

    Ab251315 is the carrier-free version of ab200657. 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

    ab251315 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.

    Maxpar® is a trademark of Fluidigm Canada Inc.

    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
    For more information see here.

    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

Images

  • Western blot - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Western blot - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Anti-Cellubrevin antibody [EPR16866] (ab200657) at 1/2000 dilution + Human fetal lung lysate at 20 µg

    Secondary
    Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution

    Predicted band size: 11 kDa
    Observed band size: 11 kDa


    Exposure time: 30 seconds


    This data was developed using ab200657, the same antibody clone in a different buffer formulation.

    Blocking and dilution buffer: 5% NFDM/TBST.

  • Western blot - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Western blot - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Anti-Cellubrevin antibody [EPR16866] (ab200657) at 1/10000 dilution + A-375 (Human malignant melanoma cell line) whole cell lysate at 10 µg

    Secondary
    Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution

    Predicted band size: 11 kDa
    Observed band size: 11 kDa


    Exposure time: 5 seconds


    This data was developed using ab200657, the same antibody clone in a different buffer formulation.

    Blocking and dilution buffer: 5% NFDM/TBST.

  • Western blot - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Western blot - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Anti-Cellubrevin antibody [EPR16866] (ab200657) at 1/10000 dilution + Human placenta tissue lysate at 10 µg

    Secondary
    Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution

    Predicted band size: 11 kDa
    Observed band size: 11 kDa


    Exposure time: 5 seconds


    This data was developed using ab200657, the same antibody clone in a different buffer formulation.

    Blocking and dilution buffer: 5% NFDM/TBST.

  • Immunocytochemistry - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Immunocytochemistry - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    This data was developed using ab200657, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized A-375 (Human malignant melanoma cell line) cells labeling Cellubrevin with ab200657 at 1/250 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Cytoplasm staining on A-375 cell line is observed. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution (red).The negative controls are as follows:
    -ve control 1: ab200657 at 1/250 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution.
    -ve control 2: ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/1000 dilution.
  • Immunocytochemistry - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Immunocytochemistry - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    This data was developed using ab200657, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized A549 (Human lung carcinoma cell line) cells labeling Cellubrevin with ab200657 at 1/250 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Cytoplasm staining on A549 cell line is observed. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution (red).The negative controls are as follows:
    -ve control 1: ab200657 at 1/250 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution.
    -ve control 2: ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/1000 dilution.
  • Flow Cytometry - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Flow Cytometry - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    This data was developed using ab200657, the same antibody clone in a different buffer formulation.Flow cytometric analysis of 2% paraformaldehyde-fixed A-375 (Human malignant melanoma cell line) cells labeling Cellubrevin with ab200657 at 1/60 dilution (red) compared with a rabbit monoclonal IgG isotype control (ab172730; black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (FITC) at 1/150 dilution was used as the secondary antibody.
  • Immunoprecipitation - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Immunoprecipitation - Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    This data was developed using ab200657, the same antibody clone in a different buffer formulation.Cellubrevin was immunoprecipitated from 1mg of A-375 (Human malignant melanoma cell line) whole cell lysate with ab200657 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab200657 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution.
    Lane 1: A-375 whole cell lysate 10µg (Input).
    Lane 2: ab200657 IP in A-375 whole cell lysate.
    Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab200657 in A-375 whole cell lysate.
    Blocking and dilution buffer and concentration: 5% NFDM/TBST.
    Exposure time: 5 seconds.
  • Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)
    Anti-Cellubrevin antibody [EPR16866] - BSA and Azide free (ab251315)

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