RFESD Antikörper (AA 51-157) (Biotin)
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- Target Alle RFESD Produkte
- RFESD (Rieske (Fe-S) Domain Containing (RFESD))
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Bindungsspezifität
- AA 51-157
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Reaktivität
- Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser RFESD Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Kreuzreaktivität
- Ratte
- Homologie
- Human,Mouse
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human RFESD
- Isotyp
- IgG
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- Applikationshinweise
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 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
- RFESD (Rieske (Fe-S) Domain Containing (RFESD))
- Andere Bezeichnung
- RFESD (RFESD Produkte)
- Synonyme
- MGC82457 antikoerper, zgc:112118 antikoerper, AI256775 antikoerper, D030068K09 antikoerper, RGD1308284 antikoerper, Rieske Fe-S domain containing antikoerper, Rieske (Fe-S) domain containing L homeolog antikoerper, Rieske (Fe-S) domain containing antikoerper, RFESD antikoerper, rfesd.L antikoerper, rfesd antikoerper, Rfesd antikoerper
- Hintergrund
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Synonyms: Rieske Fe S domain containing, Rieske domain containing protein, RFESD_HUMAN.
Background: RFESD, also known as Rieske domain-containing protein, is a 157 amino acid protein that binds one 2Fe-2S cluster per subunit. Involved in metal ion binding, RFESD contains one Rieske domain. The RFESD gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 5q15. Chromosome 5 makes up approximately 6 % of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
- Gen-ID
- 317671
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