C21orf59 Antikörper (AA 151-250) (Biotin)

Produktnummer ABIN1701472

Produktdetails anti-C21orf59 Antikörper (Biotin)

Target: C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))

Bindungsspezifität: AA 151-250

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C21orf59 Antikörper ist konjugiert mit Biotin

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Homologie: Human,Mouse,Rat,Cow,Sheep,Pig,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C21orf59

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 C21orf59

Target: C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))

Andere Bezeichnung: C21orf59 (C21orf59 Produkte)

Synonyme: C21orf59 antikoerper, MGC83493 antikoerper, C3H21orf59 antikoerper, C21orf48 antikoerper, RA_m005_jsm24C07r antikoerper, chromosome 1 open reading frame, human C21orf59 antikoerper, chromosome 21 open reading frame 59 L homeolog antikoerper, chromosome 3 C21orf59 homolog antikoerper, chromosome 21 open reading frame 59 antikoerper, chromosome 3 open reading frame, human C21orf59 antikoerper, chromosome 14 open reading frame, human C21orf59 antikoerper, C1H21ORF59 antikoerper, c21orf59.L antikoerper, C3H21orf59 antikoerper, c21orf59 antikoerper, C21orf59 antikoerper, C14H21orf59 antikoerper

Hintergrund:

Synonyms: C21orf48, C21orf59, Chromosome 21 open reading frame 59, CU059_HUMAN, FLJ20467, FLJ37137, FLJ40247, Uncharacterized protein C21orf59.

Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.

Gen-ID: 56683