×
Aktivieren Sie Javascript in Ihrem Browser, um unsere Webseite optimal zu nutzen.
SLC29A3 Antikörper (C-Term)
SLC29A3
Reaktivität: Human
WB
Wirt: Kaninchen
Polyclonal
unconjugated
Produktnummer ABIN5517444
Produktdetails anti-SLC29A3 Antikörper
(ausblenden)
Target
Alle SLC29A3 Antikörper anzeigen
SLC29A3
(Solute Carrier Family 29 Member 3 (SLC29A3))
Bindungsspezifität
Alle Epitope für SLC29A3 Antikörper
C-Term
Reaktivität
Alle Reaktivitäten für SLC29A3 Antikörper
Human
Wirt
Alle Wirte für SLC29A3 Antikörper
Kaninchen
Klonalität
Alle Klonalitäten für SLC29A3 Antikörper
Polyklonal
Konjugat
Alle Konjugate für SLC29A3 Antikörper
Dieser SLC29A3 Antikörper ist unkonjugiert
Applikation
Alle Applikationen für SLC29A3 Antikörper
Western Blotting (WB)
Sequenz
KALPGFVLLR TCLIPLFVLC NYQPRVHLKT VVFQSDVYPA LLSSLLGLSN
Homologie
Dog: 86%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Rat: 86%
Aufreinigung
Affinity purified
Immunogen
The immunogen is a synthetic peptide directed towards the C terminal region of human SLC29A3
Top Product
Discover our top product SLC29A3 Primärantikörper
Alternativen
(anzeigen)
Anwendungsinformationen
(ausblenden)
Applikationshinweise
Optimal working dilution should be determined by the investigator.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Handhabung
(ausblenden)
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.
Details zu SLC29A3
(ausblenden)
Target
SLC29A3
(Solute Carrier Family 29 Member 3 (SLC29A3))
Andere Bezeichnung
SLC29A3 (SLC29A3 Produkte )
Hintergrund
This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described. Alias Symbols: ENT3, HJCD, PHID, HCLAP Protein Size: 329
Gen-ID
55315
NCBI Accession
XM_017016377 , XP_016871866
Zuletzt angesehen
(ausblenden)