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

TPM3 Antikörper

Der Kaninchen Polyklonal Anti-TPM3-Antikörper wurde für WB, IHC, ELISA und IP validiert. Er ist geeignet, TPM3 in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN5698646

Kurzübersicht für TPM3 Antikörper (ABIN5698646)

Target

Alle TPM3 Antikörper anzeigen
TPM3 (Tropomyosin 3 (TPM3))

Reaktivität

  • 30
  • 16
  • 12
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 27
  • 6
Kaninchen

Klonalität

  • 28
  • 5
Polyklonal

Konjugat

  • 22
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser TPM3 Antikörper ist unkonjugiert

Applikation

  • 21
  • 12
  • 10
  • 7
  • 6
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunoprecipitation (IP)
  • Immunogen

    tropomyosin 3

    Isotyp

    IgG
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with FNab08890(TPM3 antibody) at dilution of 1:800

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    PBS with 0.02 % sodium azide and 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.

    Handhabung

    Avoid repeated freeze / thaw cycles.

    Lagerung

    -20 °C

    Haltbarkeit

    12 months
  • Target

    TPM3 (Tropomyosin 3 (TPM3))

    Andere Bezeichnung

    TPM3

    Hintergrund

    Synonyms:CAPM1, CFTD, HEL-189, HEL-S-82p, hscp30,NEM1, OK/SW-cl.5, TM-5,TM3, TM30, TM30nm, TM5, TPMsk3, TRK Background:This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants.

    Gen-ID

    7169

    UniProt

    P06753
Sie sind hier:
Chat with us!