SLAIN1 Antikörper (AA 1-100) (Cy3)

Produktnummer ABIN1702210

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch SLAIN1 in IF (cc) und IF (p). Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für SLAIN1 Antikörper (AA 1-100) (Cy3) (ABIN1702210)

Target: SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLAIN1 Antikörper ist konjugiert mit Cy3

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

Produktdetails anti-SLAIN1 Antikörper (Cy3)

Bindungsspezifität: AA 1-100

Homologie: Human,Mouse,Rat,Dog,Chicken,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SLAIN1/C13orf32

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 SLAIN1

Target: SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))

Andere Bezeichnung: SLAIN1

Hintergrund:

Synonyms: C13orf32, chromosome 13 open reading frame 32, FLJ30046, MGC131899, SLAI1_HUMAN, SLAIN mot family member 1, SLAIN mot family, member 1, SLAIN mot-containing protein 1, Slain1.

Background: SLAIN1 is a 561 amino acid member of the SLAIN motif-containing family and is expressed in embryonic stem cells, as well as in lung, brain and testis, where it exists as two alternatively spliced isoforms. The gene encoding SLAIN1 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4 % of the human genome. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.