LRRC33 anticorps (AA 501-600) (FITC)

N° du produit ABIN6986987

L’anticorps Lapin Polyclonal anti-LRRC33 a été validé pour WB, IF (cc) et IF (p). Il convient pour détecter LRRC33 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour LRRC33 anticorps (AA 501-600) (FITC) (ABIN6986987)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LRRC33 est conjugé à/à la FITC

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

Détail du produit anti-LRRC33 anticorps (FITC)

Épitope: AA 501-600

Réactivité croisée: Humain, Souris, Rat

Homologie: Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human LRRC33

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 LRRC33

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

Autre désignation: LRRC33

Sujet:

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.

ID gène: 375387

UniProt: Q86YC3