CRX Antikörper (N-Term)

Produktnummer ABIN2775168

Der Kaninchen Polyklonal anti-CRX Antikörper wird verwendet zum Nachweis von CRX in Proben von Human. Er wurde validiert für WB.

Kurzübersicht für CRX Antikörper (N-Term) (ABIN2775168)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CRX Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-CRX Antikörper

Bindungsspezifität: N-Term

Verwendungszweck: CRX Antibody - N-terminal region

Sequenz: VDLMHQAVPY PSPPLALDPP RRQRQERTVY TESQQKVLEF YFQKDQYPNY

Homologie: Human: 100%

Produktmerkmale: This is a rabbit polyclonal antibody against CRX. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of human CRX

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Kommentare:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP36301-100UG

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Konservierungsmittel: Sodium azide

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

Handhabung: prevent freeze-thaw cycles

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Details zu CRX

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

Andere Bezeichnung: CRX

Hintergrund:

Background Information: 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.

Gene Name: cone-rod homeobox

Alternative Symbols: CRD, LCA7, OTX3, CORD2

Protein Name: cone-rod homeobox protein

Molekulargewicht: 35kDa

Gen-ID: 1406

NCBI Accession: NP_000545

UniProt: O43186