Validated using a knockout cell line
Recombinant
RabMAb

Recombinant Anti-Pyrin antibody [EPR18676] - BSA and Azide free (ab222484)

Overview

  • Product name

    Anti-Pyrin antibody [EPR18676] - BSA and Azide free
    See all Pyrin primary antibodies
  • Description

    Rabbit monoclonal [EPR18676] to Pyrin - BSA and Azide free
  • Host species

    Rabbit
  • Tested applications

    Suitable for: WB, IPmore details
  • Species reactivity

    Reacts with: Mouse
  • Immunogen

    Recombinant fragment aa 50-450. The exact sequence is proprietary.
    Database link: Q9JJ26

  • Positive control

    • WB: Bone marrow derived-macrophage of wild type C57/B6 mice, untreated and stimulated with LPS or TNF alpha; DC2.4 stable expression whole cell lysate. IP: DC2.4 stable expression whole cell lysate.
  • General notes

    Ab222484 is the carrier-free version of ab195975. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.

     

    Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMab® patents.

    This product is a recombinant rabbit monoclonal antibody.

Properties

Applications

Our Abpromise guarantee covers the use of ab222484 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
WB Use at an assay dependent concentration. Detects a band of approximately 110 kDa (predicted molecular weight: 86 kDa).
IP Use at an assay dependent concentration.

Target

  • Function

    Probably controls the inflammatory response in myelomonocytic cells at the level of the cytoskeleton organization.
  • Tissue specificity

    Expressed in peripheral blood leukocytes, particularly in mature granulocytes and to a lesser extent in monocytes but not in lymphocytes. Detected in spleen, lung and muscle, probably as a result of leukocyte infiltration in these tissues. Not expressed in thymus, prostate, testis, ovary, small intestine, colon, heart, brain, placenta, liver, kidney, pancreas. Expression detected in several myeloid leukemic, colon cancer, and prostate cancer cell lines.
  • Involvement in disease

    Defects in MEFV are the cause of familial Mediterranean fever autosomal recessive (ARFMF) [MIM:249100]. ARFMF is an inherited disorder characterized by recurrent episodic fever, serosal inflammation and pain in the abdomen, chest or joints. ARFMF is frequently complicated by amyloidosis, which leads to renal failure and can be prophylactically treated with colchicine. ARFMF primarily affects ancestral ethnic groups living around the Mediterranean basin: North African Jews, Armenians, Arabs and Turks. The disease is also distributed in other populations including Greeks, Cypriots, Italians and Spanish, although at a lower prevalence.
    Defects in MEFV are the cause of familial Mediterranean fever autosomal dominant (ADFMF) [MIM:134610]. ADFMF is characterized by periodic fever, serosal inflammation and pain in the abdomen, chest or joints as seen also in the autosomal recessive form of the disease. It is associated with renal amyloidosis and characterized by colchicine unresponsiveness.
  • Sequence similarities

    Contains 1 B box-type zinc finger.
    Contains 1 B30.2/SPRY domain.
    Contains 1 DAPIN domain.
  • Developmental stage

    First detected in bone marrow promyelocytes. Expression increases throughout myelocyte differentiation and peaks in the mature myelomonocytic cells.
  • Cellular localization

    Nucleus and Cytoplasm > cytoskeleton. Associated with microtubules and with the filamentous actin of perinuclear filaments and peripheral lamellar ruffles.
  • Information by UniProt
  • Database links

  • Alternative names

    • FMF antibody
    • Marenostrin antibody
    • Mediterranean fever antibody
    • Mediterranean fever protein antibody
    • MEF antibody
    • Mefv antibody
    • MEFV_HUMAN antibody
    • Pyrin antibody
    • TRIM20 antibody
    see all

Images

  • Pyrin was immunoprecipitated from DC2.4 (Human immature dendritic cell line) stable Pyrin expression whole cell lysate with ab195975 at 1/100 dilution. Western blot was performed from the immunoprecipitate using ab195975 at 1/1000 dilution. Goat anti-Rabbit IgG (H+L), was used as secondary antibody at 1/5000 dilution.

    Lane 1: DC2.4 whole cell lysate.

    Lane 2: DC2.4 stable Pyrin expression whole cell lysate.

    Lane 3: DC2.4 stable Pyrin expression whole cell lysate.

    Lane 4: ab195975 IP in DC2.4 whole cell lysate.

    Lane 5: ab195975 IP in DC2.4 stable Pyrin expression whole cell lysate.

    Lane 6: Mock IP (without ab195975) in DC2.4 stable Pyrin expression whole cell lysate.

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

    Exposure time: 30 seconds.

    This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab195975).

  • All lanes : Anti-Pyrin antibody [EPR18676] (ab195975) at 1/1000 dilution

    Lane 1 : Bone marrow derived-macrophage of Pyrin -/- mice
    Lane 2 : Bone marrow derived-macrophage of Pyrin -/- mice stimulated with LPS
    Lane 3 : Bone marrow derived-macrophage of Pyrin -/- mice stimulated with TNF alpha
    Lane 4 : Bone marrow derived-macrophage of wild type C57/B6 mice
    Lane 5 : Bone marrow derived-macrophage of wild type C57/B6 mice stimulated with LPS
    Lane 6 : Bone marrow derived-macrophage of wild type C57/B6 mice stimulated with TNF alpha

    Lysates/proteins at 5 µg per lane.

    Secondary
    All lanes : Goat anti-Rabbit IgG (H+L) at 1/5000 dilution

    Predicted band size: 86 kDa
    Observed band size: 110 kDa
    why is the actual band size different from the predicted?



    This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab195975).

    Blocking/Dilution buffer: 5% milk/TBST.

References

ab222484 has not yet been referenced specifically in any publications.

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