CRX anticorps (N-Term)

N° du produit ABIN2775168

L’anticorps anti-CRX Polyclonal Lapin est utilisé pour la détection de CRX dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour CRX anticorps (N-Term) (ABIN2775168)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CRX est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-CRX anticorps

Épitope: N-Term

Fonction: CRX Antibody - N-terminal region

Séquence: VDLMHQAVPY PSPPLALDPP RRQRQERTVY TESQQKVLEF YFQKDQYPNY

Homologie: Human: 100%

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

Purification: Affinity Purified

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

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

Agent conservateur: Sodium azide

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

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur CRX

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

Autre désignation: CRX

Sujet:

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

Poids moléculaire: 35kDa

ID gène: 1406

NCBI Accession: NP_000545

UniProt: O43186