C1ORF21 Antikörper (AA 51-121) (Alexa Fluor 594)

Produktnummer ABIN2810682

Produktdetails anti-C1ORF21 Antikörper

Target: C1ORF21 (Chromosome 1 Open Reading Frame 21 (C1ORF21))

Bindungsspezifität: AA 51-121

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C1ORF21 Antikörper ist konjugiert mit Alexa Fluor 594

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

Homologie: Human,Mouse,Rat,Cow,Chicken

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf21

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.

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu C1ORF21

Target: C1ORF21 (Chromosome 1 Open Reading Frame 21 (C1ORF21))

Andere Bezeichnung: C1orf21 (C1ORF21 Produkte)

Synonyme: PIG13 antikoerper, C1orf21 antikoerper, chromosome 1 open reading frame 21 antikoerper, chromosome 8 open reading frame, human C1orf21 antikoerper, C1orf21 antikoerper, C8H1ORF21 antikoerper

Hintergrund:

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf21 gene product has been provisionally designated C1orf21 pending further characterization.

Subcellular location: Cytoplasm, Nucleus

Synonyms: C1orf21, CA021_HUMAN, Cell proliferation-inducing gene 13 protein, PIG13, RP4-768P8.1, Uncharacterized protein C1orf21.

Gen-ID: 81563