C16orf57 Antikörper (N-Term)
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- Target Alle C16orf57 (USB1) Antikörper anzeigen
- C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))
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Bindungsspezifität
- N-Term
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C16orf57 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Sequenz
- LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG
- Aufreinigung
- Affinity purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57
- Top Product
- Discover our top product USB1 Primärantikörper
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- Applikationshinweise
- Optimal working dilution should be determined by the investigator.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Target
- C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))
- Andere Bezeichnung
- C16ORF57 (USB1 Produkte)
- Synonyme
- C16orf57 antikoerper, HVSL1 antikoerper, Mpn1 antikoerper, PN antikoerper, hUsb1 antikoerper, C18H16orf57 antikoerper, AA960436 antikoerper, RGD1305215 antikoerper, c16orf57 antikoerper, C2H16orf57 antikoerper, zgc:91896 antikoerper, U6 snRNA biogenesis phosphodiesterase 1 antikoerper, U6 snRNA biogenesis 1 antikoerper, U6 snRNA biogenesis phosphodiesterase 1 L homeolog antikoerper, USB1 antikoerper, Usb1 antikoerper, usb1.L antikoerper, usb1 antikoerper
- Hintergrund
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This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
Alias Symbols: PN, Mpn1, HVSL1, hUsb1, C16orf57
Protein Size: 186 - Gen-ID
- 79650
- NCBI Accession
- NM_001195302, NP_001182231
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