LRRC33 antibody (AA 501-600) (Cy5)

Catalog No. ABIN6984404

The Rabbit Polyclonal anti-LRRC33 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect LRRC33 in samples from Human, Mouse and Rat.

Quick Overview for LRRC33 antibody (AA 501-600) (Cy5) (ABIN6984404)

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 Cy5

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

Product Details anti-LRRC33 Antibody (Cy5)

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