RP1 anticorps (AA 451-550) (Cy7)

N° du produit ABIN1406748

Détail du produit anti-RP1 anticorps (Cy7)

Antigène: RP1 (Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1))

Épitope: AA 451-550

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RP1 est conjugé à/à la Cy7

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

Homologie: Human,Mouse,Rat,Dog,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human RP1/Oxygen-regulated protein 1

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur RP1

Antigène: RP1 (Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1))

Autre désignation: Oxygen-regulated protein 1 (RP1 Produits)

Synonymes: anticorps orp1, anticorps MGC83581, anticorps DCDC4A, anticorps ORP1, anticorps Rp1h, anticorps Dcdc3, anticorps Orp1, anticorps mG145, anticorps RP1, axonemal microtubule associated L homeolog, anticorps RP1, axonemal microtubule associated, anticorps retinitis pigmentosa 1 (autosomal dominant), anticorps uncharacterized LOC100355685, anticorps retinitis pigmentosa 1 (human), anticorps rp1.L, anticorps RP1, anticorps rp1, anticorps LOC100355685, anticorps Rp1

Sujet:

Synonyms: DCDC4A, ORP1, Oxygen-regulated protein 1, Retinitis pigmentosa 1 protein, Retinitis pigmentosa RP1 protein, RP1, RP1_HUMAN.

Background: Retinitis pigmentosa 1 is a novel 2,156 amino acid oxygen-regulated photoreceptor specific to retina. Originally named ORP1 (for 'oxygen-regulated protein-1'), the expression of retinitis pigmentosa 1 has been found to be regulated by oxygen levels in the retina. Mutation of the retinitis pigmentosa 1 gene causes dominant retinitis pigmentosa which leads to degeneration of retinal photoreceptor cells and symptoms such as night vision blindness and deficits in the midperipheral visual field. Retinitis pigmentosa 1 may assist in differentiation of photoreceptor cells and has been identified in the cilia of photoreceptors, possibly aiding in both cilial structure and protein transport between inner and outer segments of photoreceptors. Retinitis pigmentosa 1 contains two doublecortin domains and is encoded by a gene which maps to human chromosome 8q11-q13.