CRX Antikörper (AA 120-285)

Produktnummer ABIN6139059

Produktdetails anti-CRX Antikörper

Target: CRX (Cone-Rod Homeobox (CRX))

Bindungsspezifität: AA 120-285

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CRX Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: KAGTSPRPST DVCPDPLGIS DSYSPPLPGP SGSPTTAVAT VSIWSPASES PLPEAQRAGL VASGPSLTSA PYAMTYAPAS AFCSSPSAYG SPSSYFSGLD PYLSPMVPQL GGPALSPLSG PSVGPSLAQS PTSLSGQSYG AYSPVDSLEF KDPTGTWKFT YNPMDP

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 120-285 of human CRX (NP_000545.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu CRX

Target: CRX (Cone-Rod Homeobox (CRX))

Andere Bezeichnung: CRX (CRX Produkte)

Synonyme: Xotx5 antikoerper, Xotx5b antikoerper, cord2 antikoerper, crd antikoerper, otx5 antikoerper, otx5b antikoerper, rx antikoerper, CRX antikoerper, crx antikoerper, otx5-b antikoerper, CORD2 antikoerper, CRD antikoerper, LCA7 antikoerper, OTX3 antikoerper, Crx1 antikoerper, otx5-A antikoerper, cone-rod homeobox antikoerper, cone-rod homeobox L homeolog antikoerper, cone-rod homeobox S homeolog antikoerper, crx antikoerper, CRX antikoerper, Crx antikoerper, crx.L antikoerper, crx.S antikoerper

Hintergrund: The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.,CRX,CORD2,CRD,LCA7,OTX3,Epigenetics & Nuclear Signaling,Transcription Factors,Neuroscience,CRX

Molekulargewicht: 32 kDa

Gen-ID: 1406

UniProt: O43186