RPS24 Antikörper (AA 83-133)
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- Target Alle RPS24 Antikörper anzeigen
- RPS24 (Ribosomal Protein S24 (RPS24))
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Bindungsspezifität
- AA 83-133
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser RPS24 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunoprecipitation (IP)
- Verwendungszweck
- Rabbit anti-RPS24 Antibody, Affinity Purified
- Homologie
- Mouse,Rat,Golden hamster
- Aufreinigung
- Affinity Purified
- Immunogen
- Between AA 83 and 133
- Isotyp
- IgG
- Top Product
- Discover our top product RPS24 Primärantikörper
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- Applikationshinweise
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IP: 2 - 10 μg/mg lysate
WB: 1:2,000 - 1:10,000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 1000 μg/mL
- Buffer
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C
- Haltbarkeit
- 12 months
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- Target
- RPS24 (Ribosomal Protein S24 (RPS24))
- Andere Bezeichnung
- RPS24 (RPS24 Produkte)
- Synonyme
- DBA3 antikoerper, S24 antikoerper, ribosomal protein S24 L homeolog antikoerper, ribosomal protein S24 antikoerper, rps24.L antikoerper, RPS24 antikoerper, Rps24 antikoerper
- Hintergrund
- Background: RPS24 (40S ribosomal protein S24) is a component of the 40S ribosomal subunit required for the processesing of pre-rRNA and maturation of the 40S ribosomal subunits. Defects in the RPS24 gene are the cause of Diamond-Blackfan anemia type 3 (DBA3) [MIM:610629]. DBA3 is a form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40 % of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies [taken from the Universal Protein Resource (UniProt) P62847].
- Gen-ID
- 6229
- NCBI Accession
- NP_001017
- UniProt
- P62847
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