Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

HAP1 Antikörper (AA 1-240)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch HAP1 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7267795

Kurzübersicht für HAP1 Antikörper (AA 1-240) (ABIN7267795)

Target

Alle HAP1 Antikörper anzeigen
HAP1 (Huntingtin Associated Protein 1 (HAP1))

Reaktivität

  • 16
  • 9
  • 8
Human

Wirt

  • 18
  • 5
  • 2
Kaninchen

Klonalität

  • 21
  • 4
Polyklonal

Konjugat

  • 22
  • 1
  • 1
  • 1
Dieser HAP1 Antikörper ist unkonjugiert

Applikation

  • 21
  • 13
  • 12
  • 11
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-240

    Verwendungszweck

    HAP1 Rabbit pAb

    Sequenz

    MRPKRLGRCC AGSRLGPGDP AALTCAPSPS ASPAPEPSAQ PQARGTGQRV GSRATSGSQF LSEARTGARP ASEAGAKAGA RRPSAFSAIQ GDVRSMPDNS DAPWTRFVFQ GPFGSRATGR GTGKAAGIWK TPAAYVGRRP GVSGPERAAF IRELEEALCP NLPPPVKKIT QEDVKVMLYL LEELLPPVWE SVTYGMVLQR ERDLNTAARI GQSLVKQNSV LMEENSKLEA LLGSAKEEIL

    Kreuzreaktivität

    Maus, Ratte

    Produktmerkmale

    Polyclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human HAP1 (NP_817084.2).

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,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

    HAP1 (Huntingtin Associated Protein 1 (HAP1))

    Andere Bezeichnung

    HAP1

    Hintergrund

    Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal proteins and a kinase substrate suggest a role for this protein in vesicular trafficking or organelle transport. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.,HAP1;HAP2;HIP5;HLP;hHLP1,Signal Transduction,Neuroscience,Neurodegenerative Diseases,HAP1

    Molekulargewicht

    66kDa/67kDa/69kDa/75kDa

    Gen-ID

    9001

    UniProt

    P54257

    Pathways

    Cell RedoxHomeostasis, Smooth Muscle Cell Migration, Positive Regulation of Response to DNA Damage Stimulus
Sie sind hier:
Chat with us!