FUNDC1 Antikörper (AA 51-150) (Cy5)

Produktnummer ABIN1704898

Produktdetails anti-FUNDC1 Antikörper (Cy5)

Target: FUNDC1 (FUN14 Domain Containing 1 (FUNDC1))

Bindungsspezifität: AA 51-150

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FUNDC1 Antikörper ist konjugiert mit Cy5

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

Kreuzreaktivität: Human, Maus, Ratte

Homologie: Dog,Cow,Sheep,Pig,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FUNDC1

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 FUNDC1

Target: FUNDC1 (FUN14 Domain Containing 1 (FUNDC1))

Andere Bezeichnung: Fundc1 (FUNDC1 Produkte)

Synonyme: fundc1-a antikoerper, 1500005J14Rik antikoerper, 1810033P05Rik antikoerper, zgc:92600 antikoerper, FUN14 domain-containing protein 1-like antikoerper, FUN14 domain containing 1 S homeolog antikoerper, FUN14 domain containing 1 antikoerper, LOC100357289 antikoerper, fundc1.S antikoerper, FUNDC1 antikoerper, Fundc1 antikoerper, fundc1 antikoerper

Hintergrund:

Synonyms: FUN14 domain containing protein 1, FUN14 domain-containing protein 1, FUND1_HUMAN.

Background: FUNDC1 is a 155 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC1 maps to human chromosome Xp11.3 and mouse chromosome X A1.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Gen-ID: 139341