C2orf68 Antikörper (Biotin)

Produktnummer ABIN1404799

Produktdetails anti-C2orf68 Antikörper (Biotin)

Target: C2orf68 (Chromosome 2 Open Reading Frame 68 (C2orf68))

Reaktivität: Maus, Human, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C2orf68 Antikörper ist konjugiert mit Biotin

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 C2orf68

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400

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 for 12 months.

Haltbarkeit: 12 months

Details zu C2orf68

Target: C2orf68 (Chromosome 2 Open Reading Frame 68 (C2orf68))

Andere Bezeichnung: C2orf68 (C2orf68 Produkte)

Synonyme: HCRCN81 antikoerper, 1500031N04Rik antikoerper, 2810411C16Rik antikoerper, AI461894 antikoerper, chromosome 2 open reading frame 68 antikoerper, chromosome 13 open reading frame, human C2orf68 antikoerper, chromosome 2 open reading frame 68 L homeolog antikoerper, RIKEN cDNA 0610030E20 gene antikoerper, chromosome 11 open reading frame, human C2orf68 antikoerper, C2orf68 antikoerper, C13H2orf68 antikoerper, c2orf68.L antikoerper, 0610030E20Rik antikoerper, C11H2orf68 antikoerper

Hintergrund:

Synonyms: Chromosome 2 open reading frame 68, FLJ14112, FLJ35653, MGC131675, CB068_HUMAN.

Background: C2orf68, also known as FLJ14112, FLJ35653 or MGC131675, is a 168 amino acid protein belonging to the UPF0561 family. Existing as two alternatively spliced isoforms, C2orf68 is encoded by a gene that maps to human chromosome 2q11.2. 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.