SSUH2 Antikörper (AA 51-150) (Alexa Fluor 594)

Produktnummer ABIN2810824

Produktdetails anti-SSUH2 Antikörper

Target: SSUH2 (Ssu-2 Homolog (C. Elegans) (SSUH2))

Bindungsspezifität: AA 51-150

Reaktivität: Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SSUH2 Antikörper ist konjugiert mit Alexa Fluor 594

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

Homologie: Human,Dog,Sheep

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf32

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 SSUH2

Target: SSUH2 (Ssu-2 Homolog (C. Elegans) (SSUH2))

Andere Bezeichnung: C3orf32 (SSUH2 Produkte)

Synonyme: C3orf32 antikoerper, SSU-2 antikoerper, fls485 antikoerper, ssu-2 homolog (C. elegans) antikoerper, SSUH2 antikoerper

Hintergrund:

C3orf32 (chromosome 3 open reading frame 32), also known as fls485, is a 353 amino acid protein encoded by a gene that maps to human chromosome 3p26.1. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.

Subcellular location: Cytoplasm

Synonyms: chromosome 3 open reading frame 32, fls485, SSU-2, SSUH2, SSUH2 ssu-2 homolog C. elegans, uncharacterized protein C3orf32 homolog, SSUH2_HUMAN.

Gen-ID: 51066