IGSF21 Antikörper (AA 90-140) (Cy5)

Produktnummer ABIN1419312

Dieses Anti-IGSF21-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von IGSF21 in WB und IF (p). Geeignet für Human, Maus und Ratte.

Kurzübersicht für IGSF21 Antikörper (AA 90-140) (Cy5) (ABIN1419312)

Target: IGSF21 (Immunoglobin Superfamily, Member 21 (IGSF21))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser IGSF21 Antikörper ist konjugiert mit Cy5

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

Produktdetails anti-IGSF21 Antikörper (Cy5)

Bindungsspezifität: AA 90-140

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human IGSF21

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: 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, 0.03 % 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 IGSF21

Target: IGSF21 (Immunoglobin Superfamily, Member 21 (IGSF21))

Andere Bezeichnung: IGSF21

Hintergrund:

Synonyms: FLJ41177, IGSF 21, Immunoglobin superfamily member 21, immunoglobulin superfamily member 21, MGC15730, RP11 121A23.1, IGS21_HUMAN, IgSF21

Background: IGSF21 is a 467 amino acid secreted protein that contains two Ig-like (immunoglobulin-like) domains and is a member of the immunoglobulin superfamily. Members of this family of proteins usually localize to the cell membrane, and may act as receptors in the immune response pathways. The gene encoding IGSF21 maps to human chromosome 1p36.13 and mouse chromosome 4 D3. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. A large number of disease-associated genes are associated with chromosome 1, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Gen-ID: 84966

UniProt: Q96ID5