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CSRP3 Antikörper

Dieses Anti-CSRP3-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von CSRP3 in WB, ELISA, IHC und IP. Geeignet für Human, Maus und Ratte.
Produktnummer ABIN5699250

Kurzübersicht für CSRP3 Antikörper (ABIN5699250)

Target

Alle CSRP3 Antikörper anzeigen
CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))

Reaktivität

  • 32
  • 19
  • 8
  • 5
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 29
  • 2
  • 1
Kaninchen

Klonalität

  • 30
  • 2
Polyklonal

Konjugat

  • 20
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser CSRP3 Antikörper ist unkonjugiert

Applikation

  • 24
  • 16
  • 6
  • 6
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunoprecipitation (IP)
  • Immunogen

    cysteine and glycine-rich protein 3 (cardiac LIM protein)

    Isotyp

    IgG
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    mouse heart tissue were subjected to SDS PAGE followed by western blot with FNab02031(CSRP3 antibody) at dilution of 1:2000

    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

    CSRP3 (Cysteine and Glycine-Rich Protein 3 (CSRP3))

    Andere Bezeichnung

    CSRP3

    Hintergrund

    Synonyms:CLP, MLP Background:This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene.

    Molekulargewicht

    21 kDa

    Gen-ID

    8048

    UniProt

    P50461
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