LRRC2 anticorps (AA 1-100) (Biotin)

N° du produit ABIN1398631

Cet anticorps Lapin Polyclonal détecte spécifiquement LRRC2 dans WB, ELISA, IHC (fro) et IHC (p). Il présente une réactivité envers Souris et Rat.

Aperçu rapide pour LRRC2 anticorps (AA 1-100) (Biotin) (ABIN1398631)

Antigène: LRRC2 (Leucine Rich Repeat Containing 2 (LRRC2))

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LRRC2 est conjugé à/à la Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-LRRC2 anticorps (Biotin)

Épitope: AA 1-100

Réactivité croisée: Souris, Rat

Homologie: Human,Dog,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human LRRC2

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Date de péremption: 12 months

Détails sur LRRC2

Antigène: LRRC2 (Leucine Rich Repeat Containing 2 (LRRC2))

Autre désignation: LRRC2

Sujet:

Synonyms: Leucine rich repeat containing 2, LRRC2_HUMAN.

Background: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 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: 79442