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TXNL4A Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch TXNL4A in WB. Er zeigt eine Reaktivität gegenüber Human und Maus.
Produktnummer ABIN6566788

Kurzübersicht für TXNL4A Antikörper (ABIN6566788)

Target

Alle TXNL4A Antikörper anzeigen
TXNL4A (Thioredoxin-Like 4A (TXNL4A))

Reaktivität

  • 8
  • 1
  • 1
Human, Maus

Wirt

  • 7
  • 1
Kaninchen

Klonalität

  • 7
  • 1
Polyklonal

Konjugat

  • 4
  • 2
  • 1
  • 1
Dieser TXNL4A Antikörper ist unkonjugiert

Applikation

  • 5
  • 3
  • 1
Western Blotting (WB)
  • Aufreinigung

    Affinity purification

    Immunogen

    Recombinant protein of human TXNL4A

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1 mg/mL

    Buffer

    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

    TXNL4A (Thioredoxin-Like 4A (TXNL4A))

    Andere Bezeichnung

    TXNL4A

    Hintergrund

    Synonyms: BMKS,DIB 1,DIB1,DIM 1,DIM1,DIM1 protein homolog,HsT161,SNRNP15,Spliceosomal U5 snRNP specific 15 kDa protein,Spliceosomal U5 snRNP-specific 15 kDa protein,Thioredoxin like 4,Thioredoxin like 4A,Thioredoxin like protein 4A,Thioredoxin like U5 snRNP protein U5 15kD,Thioredoxin-like protein 4A,Thioredoxin-like U5 snRNP protein U5-15kD,TXN4A,TXNL 4,TXNL 4A,TXNL4,txnl4a,U5 15kD

    Background: The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants.

    Molekulargewicht

    Observed_MW: 13kDa

    Calculated_MW: 16kDa

    Gen-ID

    10907

    UniProt

    P83876

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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