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Merck

MABS482

Sigma-Aldrich

Anti-PL Scramblase 1 Antibody, clone 1A8

clone 1A8, from mouse

Synonym(e):

Phospholipid scramblase 1, PL Scramblase 1, Ca(2+)-dependent phospholipid scramblase 1, Erythrocyte phospholipid scramblase, MmTRA1b

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About This Item

UNSPSC-Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Biologische Quelle

mouse

Qualitätsniveau

Antikörperform

purified antibody

Antikörper-Produkttyp

primary antibodies

Klon

1A8, monoclonal

Speziesreaktivität

human, mouse

Methode(n)

immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

Isotyp

IgG2bκ

NCBI-Hinterlegungsnummer

UniProt-Hinterlegungsnummer

Versandbedingung

wet ice

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... PLSCR1(5359)

Allgemeine Beschreibung

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.

Immunogen

Recombinant protein corresponding to human PL Scramblase 1.

Anwendung

Research Category
Zelluläre Signaltransduktion
Research Sub Category
Signalübertragung & Neurowissenschaft
Anti-PL Scramblase 1 Antibody, clone 1A8 is an antibody against PL Scramblase 1 for use in Western Blotting, Immunohistochemistry, Immunoprecipitation.
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).

Qualität

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.

Zielbeschreibung

~35 kDa observed. Uncharacterized band(s) may appear in some lysates.

Physikalische Form

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.

Lagerung und Haltbarkeit

Stable for 1 year at 2-8°C from date of receipt.

Sonstige Hinweise

Concentration: Please refer to lot specific datasheet.

Haftungsausschluss

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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Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Nuclear phospholipid scramblase 1 prolongs the mitotic expansion of granulocyte precursors during G-CSF-induced granulopoiesis.
Chen, CW; Sowden, M; Zhao, Q; Wiedmer, T; Sims, PJ
Journal of Leukocyte Biology null
Adiposity, dyslipidemia, and insulin resistance in mice with targeted deletion of phospholipid scramblase 3 (PLSCR3).
Wiedmer, T; Zhao, J; Li, L; Zhou, Q; Hevener, A; Olefsky, JM; Curtiss, LK; Sims, PJ
Proceedings of the National Academy of Sciences of the USA null
Asma Kassas et al.
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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