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Anti-SOCE-Associated Regulatory Factor

产品信息
  • Anti-SOCE-Associated Regulatory FactorStore-operated calcium entry-associated regulatory factor, SOCE-associated regulatory factor, Transmembrane protein 66, TMEM66, SARAF
    Cat #: ACC-0067
    Sizes: 25 µl, 50 µl, 0.2 ml
    Source: Rabbit
    Type: Polyclonal
    Applications: WB
    May also work in: IFC, IC, IP, IH
    Reactivity: H, M, RApplication key:CBE- Cell-based ELISA, FC- Flow cytometry, IC- Immunocytochemistry, IE- Indirect ELISA, IFC- Indirect flow cytometry, IH- Immunohistochemistry, IP- Immunoprecipitation, LCI- Live cell imaging, N- Neutralization, WB- Western blotSpecies reactivity key:H- Human, M- Mouse, R- Rat
    CLICK HERE TO RECEIVE A 25 µl FREE TRIAL SAMPLE!

    Alomone Labs is pleased to offer a highly specific antibody directed against an epitope of rat SARAF. Anti-SOCE-Associated Regulatory Factor antibody (#ACC-067) can be used in western blot analysis. It has been designed to recognize SARAF from human, rat and mouse samples.

    • Applications
    • Specifications
    • Scientific Background
    • Related Products
    Western blot

    Western blot analysis of rat pancreas (lanes 1 and 2), MS1 cells (lanes 3 and 5) and PANC1 cells (lanes 4 and 6) lysates:
    1, 3, 4. Anti-SOCE-Associated Regulatory Factor antibody (#ACC-067), (1:500).
    2, 5, 6. Anti-SOCE-Associated Regulatory Factor antibody, preincubated with the control peptide antigen.
    Immunogen
    Peptide (C)ELGLSKLKESGKHQS, corresponding to amino acid residues 141-155 of rat SOCE-associated regulatory factor (Accession Q6AYN2). Intracellular, lumen.

    HomologyMouse - 13/15 amino acid residues identical; human - 11/15 amino acid residues identical.
    PurityAffinity purified on immobilized antigen.
    FormulationLyophilized powder. Reconstituted antibody contains phosphate buffered saline (PBS), pH 7.4, 1% BSA, 0.05% NaN3.
    Standard quality control of each lotWestern blot analysis.
    Peptide confirmationConfirmed by amino acid analysis and mass spectrometry.
    Storage before reconstitutionThe antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C.
    Reconstitution25 µl, 50 µl or 0.2 ml double distilled water (DDW), depending on the sample size.
    Antibody concentration after reconstitution0.85 mg/ml.
    Storage after reconstitutionThe reconstituted solution can be stored at 4°C for up to 1 week. For longer periods, small aliquots should be stored at -20°C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).
    Control antigen storage before reconstitutionLyophilized powder can be stored intact at room temperature for 2 weeks. For longer periods, it should be stored at -20°C.
    Control antigen reconstitution100 µl double distilled water (DDW).
    Control antigen storage after reconstitution-20ºC.
    Preadsorption Control1 µg peptide per 1 µg antibody.
    Scientific background

    SOCE-associated regulatory factor (SARAF) is a regulatory protein of cellular Ca2+ homeostasis, encoded by the TMEM66 gene. SARAF is an ER resident protein, which responds to cytosolic Ca2+ elevation after ER Ca2+ refilling.

    SARAF is highly conserved in vertebrates, and in mammals it is ubiquitously expressed with high transcript levels in the immune and neuronal tissues. SARAF structure contains validated signal peptide and a putative single membrane spanning domain, a serine-proline rich domain and arginine rich regions followed by a cluster of basic residues at its C-terminal tail1.

    Store-operated Ca2+ entry (SOCE) is an important Ca2+ influx pathway across plasma membrane in many non-excitable cells. In this pathway, intracellular Ca2+ release through IP3 receptor stimulated by a variety of agonists, results in reduction of Ca2+ concentration in the lumen of endoplasmic or sarcoplasmic reticulum. SARAF negatively regulates store operated calcium entry into cells and protects cells from calcium overfilling1,2.

    STIM, Ca2+ sensor, and Orai, the channel pore forming subunit proteins have been identified as the essential components enabling the reconstitution of Ca2+ release-activated Ca2+ channels that mediate SOCE. Knock-out of Orai1 or STIM1 in mice and mutations evoke SOCE in lymphocytes and other cells2,3.

    Several findings show that dysregulation of Ca2+ homeostasis is associated with a plethora of pathological conditions including neurodegenerative diseases, skeletal, muscular and cardiovascular disorders2. Inherited defects in SOCE due to mutations in genes of the Ca2+ release-activated Ca2+ (CRAC) channel complex causes patients to suffer from a severe form of immunodeficiency that is due to defects in the function of T cells, NK cells and potentially other immune cells3.


    References
    1. Palty, R. et al. (2012) Cell 149, 425.
    2. Pan, Z. et al. (2014) BMB Rep. 47, 69.
    3. Feske, S. (2011) Ann. N Y Acad. Sci. 1238, 74.
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