推荐产品
生物源
mouse
品質等級
抗體表格
purified antibody
抗體產品種類
primary antibodies
無性繁殖
1A8, monoclonal
物種活性
human, mouse
技術
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
同型
IgG2bκ
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
目標翻譯後修改
unmodified
基因資訊
human ... PLSCR1(5359)
一般說明
Phospholipid scramblase 1 (UniProt O15162; also known as Ca(2+)-dependent phospholipid scramblase 1, Erythrocyte phospholipid scramblase, MmTRA1b, PL scramblase 1) is encoded by the PLSCR1 (also known as MMTRA1B) gene (Gene ID 5359) in human. Plasma membrane phospholipids are distributed asymmetrically between the inner and outer leaflets. Such asymmetrical distribution collapses in response to blood coagulation and apoptosis, resulting in phospholipid “scrambling” between the two leaflets of the plasma membrane. Flippases, floppases, and scramblases are three types enzymes known to mediate transbilayer lipid motion. Flippases and floppases function via ATP-dependent mechanism, while scramblases mediate transbilayer movement in a non-selective and energy-independent manner. Originally identified in 1996 as a 37 kDa erythrocyte type II transmembrane protein that mediates calcium-dependent membrane phospholipids redistribution, PL Scramblase 1 is the protein product encoded by the founding member of the PLSCR family of genes (PLSCR1-5). All PLSCR family members, with the exception of PLSCR2, possess a proline-rich N-terminal region containing PxxP and PPxY domains, a cysteine-rich region, a conserved calcium-binding domain (EF-hand-like), and a putative transmembrane region enriched in hydrophobic amino acids. In addition, PLSCR1 contains a nuclear localization signal (NLS) and a DNA-binding domain that are essential for its nuclear localization and associated nuclear function. In addition to PLSCRs, TMEM16 and XKR family members have also been reported to mediate scramblase activity.
免疫原
Recombinant protein corresponding to human PL Scramblase 1.
應用
Anti-PL Scramblase 1 Antibody, clone 1A8 is an antibody against PL Scramblase 1 for use in Western Blotting, Immunohistochemistry, Immunoprecipitation.
Research Category
Signaling
Signaling
Research Sub Category
Signaling Neuroscience
Signaling Neuroscience
Western Blotting Analysis: 1.0 µg/mL from a representative lot detected PL Scramblase 1 in 10 µg of A549 cell lysate.
Immunohistochemistry Analysis: A 1:50 dilution from a representative lot detected PL Scramblase 1 in mouse colon tissue.
Western Blotting Analysis: A representative lot detected PL scramblase 1 in platelets and lung tissue from wild-type and PLSCR3-/-, but not PLSCR1-/-, mice, while little or no PL scramblase 1 was detected in adipocyte or muscle samples from wild-type or the knockout animals (Wiedmer, T., et al. (2004). Proc Natl Acad Sci USA. 101(36):13296-13301).
Western Blotting Analysis: A representative lot detected retroviral-mediated ectopic expression of murine PLSCR1 in SCF-ER-Hoxb8-immortalized myeloid progenitor cells from PLSCR1−/− mice (Chen, C.W., et al. (2011). J Leukoc Biol. 90(2):221-233).
Immunprecipitation Analysis: A representative lot immunoprecipitated PL scramblase 1 from murine bone marrow-derived mast cells (BMMCs) following IgE receptor activation. Tyrosine phosphorylation of PL scramblase 1 was then checked by Western blotting with clone 4G10 (Kassas, A., et al. (2014). PLoS One. 9(10):e109800).
Immunohistochemistry Analysis: A 1:50 dilution from a representative lot detected PL Scramblase 1 in mouse colon tissue.
Western Blotting Analysis: A representative lot detected PL scramblase 1 in platelets and lung tissue from wild-type and PLSCR3-/-, but not PLSCR1-/-, mice, while little or no PL scramblase 1 was detected in adipocyte or muscle samples from wild-type or the knockout animals (Wiedmer, T., et al. (2004). Proc Natl Acad Sci USA. 101(36):13296-13301).
Western Blotting Analysis: A representative lot detected retroviral-mediated ectopic expression of murine PLSCR1 in SCF-ER-Hoxb8-immortalized myeloid progenitor cells from PLSCR1−/− mice (Chen, C.W., et al. (2011). J Leukoc Biol. 90(2):221-233).
Immunprecipitation Analysis: A representative lot immunoprecipitated PL scramblase 1 from murine bone marrow-derived mast cells (BMMCs) following IgE receptor activation. Tyrosine phosphorylation of PL scramblase 1 was then checked by Western blotting with clone 4G10 (Kassas, A., et al. (2014). PLoS One. 9(10):e109800).
品質
Evaluated by Western Blotting in HeLa cell lysate.
Western Blotting Analysis: 1.0 µg/mL of this antibody detected PL Scramblase 1 in 10 µg of HeLa cell lysate.
Western Blotting Analysis: 1.0 µg/mL of this antibody detected PL Scramblase 1 in 10 µg of HeLa cell lysate.
標靶描述
~35 kDa observed. Uncharacterized band(s) may appear in some lysates.
外觀
Protein G Purified
Format: Purified
Purified mouse monoclonal IgG2bκ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
儲存和穩定性
Stable for 1 year at 2-8°C from date of receipt.
其他說明
Concentration: Please refer to lot specific datasheet.
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
Nuclear phospholipid scramblase 1 prolongs the mitotic expansion of granulocyte precursors during G-CSF-induced granulopoiesis.
Journal of Leukocyte Biology null
Adiposity, dyslipidemia, and insulin resistance in mice with targeted deletion of phospholipid scramblase 3 (PLSCR3).
Proceedings of the National Academy of Sciences of the USA null
PloS one, 9(10), e109800-e109800 (2014-10-08)
Engagement of high-affinity immunoglobulin E receptors (FcεRI) activates two signaling pathways in mast cells. The Lyn pathway leads to recruitment of Syk and to calcium mobilization whereas the Fyn pathway leads to phosphatidylinositol 3-kinase recruitment. Mapping the connections between both
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