RP1 antibody (AA 451-550) (Cy5.5)

Catalog No. ABIN1406747

Product Details anti-RP1 Antibody (Cy5.5)

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

Binding Specificity: AA 451-550

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RP1 antibody is conjugated to Cy5.5

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

Predicted Reactivity: Human,Mouse,Rat,Dog,Horse,Rabbit

Purification: Purified by Protein A.

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

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for RP1

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

Alternative Name: Oxygen-regulated protein 1 (RP1 Products)

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

Background:

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.