SNRNP200 Polyklonaler Antikörper

SNRNP200 Polyklonal Antikörper für FC (Intra)

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus

Anwendung

FC (Intra)

Konjugation

PE Fluorescent Dye

Kat-Nr. : PE-23875

Synonyme

KIAA0788, HELIC2, EC:3.6.4.13, BRR2, ASCC3L1



Geprüfte Anwendungen

Erfolgreiche Detektion in FC (Intra)A431-Zellen

Empfohlene Verdünnung

AnwendungVerdünnung
Durchflusszytometrie (FC) (INTRA)FC (INTRA) : 0.20 ug per 10^6 cells in a 100 µl suspension
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

PE-23875 bindet in FC (Intra) SNRNP200 und zeigt Reaktivität mit human, Maus

Getestete Reaktivität human, Maus
Wirt / Isotyp Kaninchen / IgG
Klonalität Polyklonal
Typ Antikörper
Immunogen SNRNP200 fusion protein Ag20748
Vollständiger Name small nuclear ribonucleoprotein 200kDa (U5)
Berechnetes Molekulargewicht 494 aa, 57 kDa
Beobachtetes Molekulargewicht 200-245 kDa
GenBank-ZugangsnummerBC001417
Gene symbol SNRNP200
Gene ID (NCBI) 23020
Konjugation PE Fluorescent Dye
Excitation/Emission maxima wavelengths496 nm, 565 nm / 578 nm
Form Liquid
Reinigungsmethode Antigen-Affinitätsreinigung
Lagerungspuffer PBS with 0.09% sodium azide and 0.5% BSA
LagerungsbedingungenStore at 2-8°C. Avoid exposure to light. Stable for one year after shipment. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

SNRNP200 (small nuclear ribonucleoprotein 200kDa (U5)), also known as HELIC2, ASCC3L1 or BRR2, is a 2,136 amino acid protein that localizes to the nucleus and contains two SEC63 domains, two helicase C-terminal domains and two helicase ATP-binding domains. Existing as multiple alternatively spliced isoforms, HELIC2 functions as an RNA helicase that is thought to promote specific RNA-RNA conformational changes which are important in the second step of RNA splicing. The gene encoding HELIC2 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the chromosome 2-localized ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes, hich also map to chromosome 2. The observed molecular weight of SNRNP200 is 200-245kd.

Protokolle

PRODUKTSPEZIFISCHE PROTOKOLLE
FC protocol for PE SNRNP200 antibody PE-23875Download protocol
STANDARD-PROTOKOLLE
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