LRRC33 antibody (AA 501-600) (AbBy Fluor® 647)

Catalog No. ABIN6980121

This anti-LRRC33 antibody is a Rabbit Polyclonal antibody detecting LRRC33 in WB, IF (cc) and IF (p). Suitable for Human, Mouse and Rat.

Quick Overview for LRRC33 antibody (AA 501-600) (AbBy Fluor® 647) (ABIN6980121)

Target: LRRC33 (NRROS) (Negative Regulator of Reactive Oxygen Species (NRROS))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LRRC33 antibody is conjugated to AbBy Fluor® 647

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

Product Details anti-LRRC33 Antibody (AbBy Fluor® 647)

Binding Specificity: AA 501-600

Cross-Reactivity: Human, Mouse, Rat

Predicted Reactivity: Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human LRRC33

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 LRRC33

Target: LRRC33 (NRROS) (Negative Regulator of Reactive Oxygen Species (NRROS))

Alternative Name: LRRC33

Background:

Synonyms: ELLP3030, GARPL1, NRROS_HUMAN, Leucine rich repeat containing protein 33, Lrcc33, UNQ3030.

Background: LRRC33 is a 692 amino acid protein that contains 17 LRR repeats. The gene encoding LRRC33 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.

Gene ID: 375387

UniProt: Q86YC3