CRB1 Antikörper (AA 301-400) (Cy7)

Produktnummer ABIN6942651

Produktdetails anti-CRB1 Antikörper (Cy7)

Target: CRB1 (Crumbs Homolog 1 (CRB1))

Bindungsspezifität: AA 301-400

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CRB1 Antikörper ist konjugiert mit Cy7

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

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CRB1

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 CRB1

Target: CRB1 (Crumbs Homolog 1 (CRB1))

Andere Bezeichnung: CRB1 (CRB1 Produkte)

Synonyme: CRB1 antikoerper, si:dkey-114d20.6 antikoerper, si:dkey-114d20.7 antikoerper, LCA8 antikoerper, RP12 antikoerper, 7530426H14Rik antikoerper, A930008G09Rik antikoerper, crumbs 1, cell polarity complex component antikoerper, crumbs family member 1, photoreceptor morphogenesis associated antikoerper, CRB1 antikoerper, crb1 antikoerper, Crb1 antikoerper

Hintergrund:

Synonyms: CRB1, CRUM1_HUMAN, Protein crumbs homolog 1.

Background: This gene encodes a protein which is similar to the Drosophila crumbs protein and localizes to the inner segment of mammalian photoreceptors. In Drosophila crumbs localizes to the stalk of the fly photoreceptor and may be a component of the molecular scaffold that controls proper development of polarity in the eye. Mutations in this gene are associated with a severe form of retinitis pigmentosa, RP12, and with Leber congenital amaurosis. Alternate splicing results in multiple transcript variants, some protein coding and some non-protein coding.[provided by RefSeq, Apr 2012]

Gen-ID: 23418

UniProt: P82279

Pathways: Notch Signalweg