TM9SF4 Antikörper (AA 101-200) (Cy5)

Produktnummer ABIN1416336

This anti-TM9SF4 antibody (ABIN1416336) is a Rabbit Polyclonal antibody detecting TM9SF4 in WB, IF (cc), IF (p). Suitable for Mouse.

Kurzübersicht für TM9SF4 Antikörper (AA 101-200) (Cy5) (ABIN1416336)

Target: TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))

Reaktivität: Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TM9SF4 Antikörper ist konjugiert mit Cy5

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

Produktdetails anti-TM9SF4 Antikörper (Cy5)

Bindungsspezifität: AA 101-200

Kreuzreaktivität: Maus

Homologie: Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TM9SF4

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 TM9SF4

Target: TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))

Andere Bezeichnung: TM9SF4

Hintergrund:

Synonyms: dJ836N17.2, Transmembrane 9 superfamily member 4, TM9SF4, KIAA0255

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis which are thought important for seminal production and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20.

Gen-ID: 9777

UniProt: Q92544