C2ORF61 Antikörper (AA 21-120) (FITC)

Produktnummer ABIN1710204

Dieses Anti-C2ORF61-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von C2ORF61 in WB, IF (cc) und IF (p). Geeignet für Human.

Kurzübersicht für C2ORF61 Antikörper (AA 21-120) (FITC) (ABIN1710204)

Target: C2ORF61 (Chromosome 2 Open Reading Frame 61 (C2ORF61))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C2ORF61 Antikörper ist konjugiert mit FITC

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-C2ORF61 Antikörper (FITC)

Bindungsspezifität: AA 21-120

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C2orf61

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Details zu C2ORF61

Target: C2ORF61 (Chromosome 2 Open Reading Frame 61 (C2ORF61))

Andere Bezeichnung: C2orf61

Hintergrund:

Synonyms: CCDC113, Chromosome 2 open reading frame 61, Coiled-coil domain-containing protein 113 Gene names, DKFZp434N1418, HSPC065, Uncharacterized protein C2orf61, CB061_HUMAN.

Background: C2orf61 (chromosome 2 open reading frame 61), also known as FLJ40172, is a 177 amino acid protein encoded by a gene that maps to human chromosome 2p21. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare 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 related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

Gen-ID: 285051