CXorf21 Antikörper (AA 165-215) (Cy5.5)

Produktnummer ABIN1421251

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch CXorf21 in FACS und IF (p). Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für CXorf21 Antikörper (AA 165-215) (Cy5.5) (ABIN1421251)

Target: CXorf21 (TASL) (TLR Adaptor Interacting With Endolysosomal SLC15A4 (TASL))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CXorf21 Antikörper ist konjugiert mit Cy5.5

Applikation: Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-CXorf21 Antikörper (Cy5.5)

Bindungsspezifität: AA 165-215

Verwendungszweck: CXorf21 Polyclonal Antibody, Cy5.5 Conjugated

Kreuzreaktivität: Human

Homologie: Mouse,Rat,Dog,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CXorf21

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: FCM(1:300-5000), IF(IHC-P)(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, 0.02 % 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 CXorf21

Target: CXorf21 (TASL) (TLR Adaptor Interacting With Endolysosomal SLC15A4 (TASL))

Andere Bezeichnung: CXorf21

Hintergrund:

Synonyms: Chromosome X open reading frame 21, FLJ11577, Hypothetical protein LOC80231, Uncharacterized protein CXorf21, CX021_HUMAN.

Background: 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. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. 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. The CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.

Gen-ID: 80231

UniProt: Q9HAI6