ANKS3 Antikörper

Produktnummer ABIN1386930

Produktdetails anti-ANKS3 Antikörper

Target: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ANKS3 Antikörper ist unkonjugiert

Applikation: Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human ANKS3

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC-P 1:200-400
IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 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: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu ANKS3

Target: ANKS3 (Ankyrin Repeat and SAM Domain-Containing Protein 3 (ANKS3))

Andere Bezeichnung: ANKS3 (ANKS3 Produkte)

Synonyme: 2700067D09Rik antikoerper, C81345 antikoerper, mKIAA1977 antikoerper, RGD1305833 antikoerper, ankyrin repeat and sterile alpha motif domain containing 3 antikoerper, anks3 antikoerper, ANKS3 antikoerper, Anks3 antikoerper

Hintergrund:

Synonyms: Ankyrin repeat and SAM domain containing protein 3, Ankyrin repeat and sterile alpha mot domain containing 3, KIAA1977, ANKS3_HUMAN.

Background: ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Gen-ID: 124401