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Lipin 1 Antikörper (AA 90-886)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Lipin 1 in WB, ELISA, ICC, IF und FACS. Er zeigt eine Reaktivität gegenüber Human und Ratte.
Produktnummer ABIN7602648

Kurzübersicht für Lipin 1 Antikörper (AA 90-886) (ABIN7602648)

Target

Alle Lipin 1 (LPIN1) Antikörper anzeigen
Lipin 1 (LPIN1)

Reaktivität

  • 54
  • 39
  • 35
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Ratte

Wirt

  • 76
  • 9
  • 3
Kaninchen

Klonalität

  • 70
  • 18
Polyklonal

Konjugat

  • 32
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Dieser Lipin 1 Antikörper ist unkonjugiert

Applikation

  • 39
  • 39
  • 24
  • 17
  • 14
  • 14
  • 9
  • 9
  • 9
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (IF), Flow Cytometry (FACS)
  • Bindungsspezifität

    • 15
    • 15
    • 15
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 90-886

    Verwendungszweck

    Anti-Lipin 1/LPIN1 Antibody Picoband®

    Kreuzreaktivität (Details)

    No cross-reactivity with other proteins.

    Produktmerkmale

    Anti-Lipin 1/LPIN1 Antibody Picoband® (ABIN7602648). Tested in ELISA, Flow Cytometry, IF, ICC, WB applications. This antibody reacts with Human, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Aufreinigung

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human Lipin 1/LPIN1 recombinant protein (Position: Q90-H886).

    Isotyp

    IgG
  • Applikationshinweise

    Western blot, 0.25-0.5 μg/mL, Human, Rat
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Cao, H., Hegele, R. A. Identification of single-nucleotide polymorphisms in the human LPIN1 gene. J. Hum. Genet. 47: 370-372, 2002. 2. Han, G.-S., Wu, W.-I., Carman, G. M. The Saccharomyces cerevisiae lipin homolog is a Mg(2+)-dependent phosphatidate phosphatase enzyme. J. Biol. Chem. 281: 9210-9218, 2006. 3. Han, S., Bahmanyar, S., Zhang, P., Grishin, N., Oegema, K., Crooke, R., Graham, M., Reue, K., Dixon, J. E., Goodman, J. M. Nuclear envelope phosphatase 1-regulatory subunit 1 (formerly TMEM188) is the metazoan Spo7p ortholog and functions in the lipin activation pathway. J. Biol. Chem. 287: 3123-3137, 2012.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Konzentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    Lipin 1 (LPIN1)

    Andere Bezeichnung

    LPIN1

    Hintergrund

    Synonyms: Probable ATP-dependent RNA helicase DDX4, DEAD box protein 4, Vasa homolog, DDX4, VASA

    Tissue Specificity: Expressed only in ovary and testis. Expressed in migratory primordial germ cells in the region of the gonadal ridge in both sexes.

    Background: This gene encodes a magnesium-ion-dependent phosphatidic acid phosphohydrolase enzyme that catalyzes the penultimate step in triglyceride synthesis including the dephosphorylation of phosphatidic acid to yield diacylglycerol. Expression of this gene is required for adipocyte differentiation and it also functions as a nuclear transcriptional coactivator with some peroxisome proliferator-activated receptors to modulate expression of other genes involved in lipid metabolism. Mutations in this gene are associated with metabolic syndrome, type 2 diabetes, acute recurrent rhabdomyolysis, and autosomal recessive acute recurrent myoglobinuria (ARARM). This gene is also a candidate for several human lipodystrophy syndromes.

    Molekulargewicht

    130 kDa

    Gen-ID

    23175

    UniProt

    Q14693

    Pathways

    Monocarboxylic Acid Catabolic Process
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