IQCA1 Antikörper (Cy3)
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- Target Alle IQCA1 Antikörper anzeigen
- IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
- Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser IQCA1 Antikörper ist konjugiert mit Cy3
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Applikation
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human IQCA1
- Isotyp
- IgG
- Top Product
- Discover our top product IQCA1 Primärantikörper
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- Applikationshinweise
- IF(IHC-P) 1:50-200
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
- Andere Bezeichnung
- IQCA1 (IQCA1 Produkte)
- Synonyme
- 4930465P12Rik antikoerper, 4930585L22Rik antikoerper, BB288505 antikoerper, Iqca1 antikoerper, IQCA antikoerper, RGD1305311 antikoerper, IQ motif containing with AAA domain antikoerper, IQ motif containing with AAA domain 1 antikoerper, Iqca antikoerper, IQCA1 antikoerper, Iqca1 antikoerper
- Hintergrund
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Synonyms: IQ and AAA domain-containing protein 1, IQ mot containing with AAA domain 1, IQCA, Iqca1, IQCA1_HUMAN, RGD1305311, FLJ22527, 4930465P12Rik, FLJ33588.
Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
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