CCDC22 Antikörper (AA 525-627) (Alexa Fluor 647)

Produktnummer ABIN887517

Produktdetails anti-CCDC22 Antikörper

Target: CCDC22 (Coiled-Coil Domain Containing 22 (CCDC22))

Bindungsspezifität: AA 525-627

Reaktivität: Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC22 Antikörper ist konjugiert mit Alexa Fluor 647

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

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCDC22

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/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu CCDC22

Target: CCDC22 (Coiled-Coil Domain Containing 22 (CCDC22))

Andere Bezeichnung: CCDC22 (CCDC22 Produkte)

Synonyme: CXorf37 antikoerper, AI481216 antikoerper, DXImx40e antikoerper, Ppp1r3f antikoerper, Sfc22 antikoerper, RGD1560910 antikoerper, zgc:114058 antikoerper, coiled-coil domain containing 22 antikoerper, CCDC22 antikoerper, Ccdc22 antikoerper, ccdc22 antikoerper

Hintergrund:

This gene encodes a protein containing a coiled-coil domain. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. Localization of the orthologous rat protein suggests that it may play a role in neuronal injury response. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2011].

Subcellular location: Cytoplasm, Nucleus, Secreted, Extracellular matrix

Synonyms: AI481216, CCD22_HUMAN, Ccdc22.

Gen-ID: 28952