FSD2 Antikörper (AA 221-320) (Alexa Fluor 594)

Produktnummer ABIN2813407

Produktdetails anti-FSD2 Antikörper

Target: FSD2 (Fibronectin Type III and SPRY Domain Containing 2 (FSD2))

Bindungsspezifität: AA 221-320

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FSD2 Antikörper ist konjugiert mit Alexa Fluor 594

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

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FSD2

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 FSD2

Target: FSD2 (Fibronectin Type III and SPRY Domain Containing 2 (FSD2))

Andere Bezeichnung: FSD2 (FSD2 Produkte)

Synonyme: SPRYD1 antikoerper, 9830160G03Rik antikoerper, Spryd1 antikoerper, RGD1305167 antikoerper, fibronectin type III and SPRY domain containing 2 antikoerper, FSD2 antikoerper, Fsd2 antikoerper

Hintergrund:

FSD2 is a 749 amino acid protein containing one B30.2/SPRY domain and two fibronectin type-III domains. The gene encoding FSD2 maps to human chromosome 15q25.2. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and consists of about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are also associated with chromosome 15.

Subcellular location: Cytoplasm, Nucleus

Synonyms: Fibronectin type III and SPRY domain containing 2, Fibronectin type III and SPRY domain containing protein 2, RP11-127F21, SPRY domain containing 1, SPRY domain containing protein 1, SPRYD1,

Gen-ID: 123722