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Lipin 1 Antikörper

Dieses Kaninchen Monoklonal-Antikörper erkennt spezifisch Lipin 1 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7268281

Kurzübersicht für Lipin 1 Antikörper (ABIN7268281)

Target

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

Reaktivität

  • 55
  • 39
  • 36
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 77
  • 9
  • 3
Kaninchen

Klonalität

  • 71
  • 18
Monoklonal

Konjugat

  • 33
  • 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
  • 25
  • 18
  • 14
  • 14
  • 10
  • 9
  • 9
  • 6
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Verwendungszweck

    Lipin 1 Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Lipin 1

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Lipin 1 (LPIN1)

    Andere Bezeichnung

    LPIN1

    Hintergrund

    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. [provided by RefSeq, Mar 2017],PAP1,Cardiovascular,Cardiovascular diseases,Cardiovascular diseases_Heart disease,Cell Biology & Developmental Biology,Cell Cycle,Cell Cycle_Cell differentiation,Endocrine & Metabolism,Endocrine and metabolic diseases,Endocrine and metabolic diseases_Diabetes,Heart,Lipid Metabolism,Lipid Metabolism_Cholesterol Metabolism,Lipids,Signal Transduction,LPIN1

    Molekulargewicht

    130kDa

    Gen-ID

    23175

    UniProt

    Q14693

    Pathways

    Monocarboxylic Acid Catabolic Process
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