SIX6OS1 Polyklonaler Antikörper

SIX6OS1 Polyklonal Antikörper für WB, ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human

Anwendung

WB, ELISA

Konjugation

Unkonjugiert

Kat-Nr. : 30610-1-AP

Synonyme

C14orf39, Protein SIX6OS1, Six6 opposite strand transcript 1

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  WB analysis using 30610-1-AP

  Various lysates were subjected to SDS PAGE followed by western blot with 30610-1-AP (SIX6OS1 antibody) at dilution of 1:4000 incubated at room temperature for 1.5 hours.

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Geprüfte Anwendungen

• Erfolgreiche Detektion in WB: COLO 320-Zellen, Jurkat-Zellen, SGC-7901-Zellen

Empfohlene Verdünnung

• Western Blot (WB): WB : 1:1000-1:8000

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, check data in validation data gallery

Produktinformation

30610-1-AP bindet in WB, ELISA SIX6OS1 und zeigt Reaktivität mit human

• Getestete Reaktivität: human
• Wirt / Isotyp: Kaninchen / IgG
• Klonalität: Polyklonal
• Typ: Antikörper
• Immunogen: SIX6OS1 fusion protein Ag33548
• Vollständiger Name: chromosome 14 open reading frame 39
• Berechnetes Molekulargewicht: 587 aa, 68 kDa
• Beobachtetes Molekulargewicht: 70 kDa
• GenBank-Zugangsnummer: BC125070
• Gene symbol: C14orf39
• Gene ID (NCBI): 317761
• Konjugation: Unkonjugiert
• Form: Liquid
• Reinigungsmethode: Antigen-Affinitätsreinigung
• Lagerungspuffer: PBS with 0.02% sodium azide and 50% glycerol
• Lagerungsbedingungen: Bei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20^oC Lagerung nicht notwendig. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

SIX6OS1 (SIX6 Opposite Strand 1) is a nuclear protein that plays a core role in the process of meiosis. It is a key scaffold protein that constitutes the central element of the synaptonemal complex, directly interacting with proteins such as SYCE1 to ensure the proper pairing, synapsis, and genetic recombination of homologous chromosomes. Its function is crucial for the formation of stable chiasmata, which are the basis for genetic diversity and the accurate segregation of chromosomes. Mutations in the SIX6OS1 gene can disrupt this process, leading to errors in chromosome separation and are one of the important genetic factors causing primary ovarian insufficiency in humans and non-obstructive azoospermia in males, directly associated with reproductive disorders.