CNOT11 Antikörper (AbBy Fluor® 647)

Produktnummer ABIN1404864

Produktdetails anti-CNOT11 Antikörper (AbBy Fluor® 647)

Target: CNOT11 (CCR4-NOT Transcription Complex, Subunit 11 (CNOT11))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CNOT11 Antikörper ist konjugiert mit AbBy Fluor® 647

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 C2orf29

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 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 CNOT11

Target: CNOT11 (CCR4-NOT Transcription Complex, Subunit 11 (CNOT11))

Andere Bezeichnung: C2orf29 (CNOT11 Produkte)

Synonyme: C2orf29 antikoerper, 2410015L18Rik antikoerper, C40 antikoerper, D1Bwg0212e antikoerper, RGD1560909 antikoerper, fj49e01 antikoerper, wu:fj49e01 antikoerper, zgc:163002 antikoerper, CCR4-NOT transcription complex subunit 11 antikoerper, CCR4-NOT transcription complex, subunit 11 antikoerper, CNOT11 antikoerper, Cnot11 antikoerper, cnot11 antikoerper

Hintergrund:

Synonyms: C2orf29, C40, CB029_HUMAN, Chromosome 2 open reading frame 29, Hypothetical protein LOC55571, UPF0760 protein C2orf29.

Background: C2orf29, also known as C40, is a 510 amino acid protein that belongs to the UPF0760 family and 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.

Gen-ID: 55571