RPUSD2 Antikörper (Biotin)
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- Target Alle RPUSD2 Produkte
- RPUSD2 (RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser RPUSD2 Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human RPUSD2
- Isotyp
- IgG
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- Applikationshinweise
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WB 1:300-5000
IHC-P 1:200-400 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C for 12 months.
- Haltbarkeit
- 12 months
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- Target
- RPUSD2 (RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2))
- Andere Bezeichnung
- RPUSD2 (RPUSD2 Produkte)
- Synonyme
- RPUSD2 antikoerper, C15orf19 antikoerper, C18B11 antikoerper, 4921503C21Rik antikoerper, 9630001E10 antikoerper, BB231107 antikoerper, RGD1306147 antikoerper, RNA pseudouridylate synthase domain containing 2 antikoerper, RPUSD2 antikoerper, Rpusd2 antikoerper
- Hintergrund
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Synonyms: C15orf19, C18B11, C18B11 homolog, RNA pseudouridylate synthase domain containing 2, RNA pseudouridylate synthase domain containing protein 2, RNA pseudouridylate synthase domain-containing protein 2, RPUSD 2, RPUSD-2, RUSD2_HUMAN.
Background: RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
- Gen-ID
- 27079
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