LRRC41 anticorps (AA 331-430) (FITC)

N° du produit ABIN1398644

Détail du produit anti-LRRC41 anticorps (FITC)

Antigène: LRRC41 (Leucine Rich Repeat Containing 41 (LRRC41))

Épitope: AA 331-430

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LRRC41 est conjugé à/à la FITC

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

Réactivité croisée: Humain, Souris, Rat

Homologie: Dog,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human LRRC41

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 LRRC41

Antigène: LRRC41 (Leucine Rich Repeat Containing 41 (LRRC41))

Autre désignation: LRRC41 (LRRC41 Produits)

Synonymes: anticorps LRRC41, anticorps MUF1, anticorps RP4-636H5.2, anticorps AA409966, anticorps AW555107, anticorps D630045E04Rik, anticorps D730026A16Rik, anticorps RGD1311221, anticorps MGC137526, anticorps leucine rich repeat containing 41, anticorps leucine-rich repeat-containing protein 41, anticorps LRRC41, anticorps lrrc41, anticorps LOC100550348, anticorps Lrrc41

Sujet:

Synonyms: elongin BC interacting leucine rich repeat protein, Leucine rich repeat containing 41, Leucine rich repeat containing protein 41, MUF1, PP7759, LRC41_HUMAN.

Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

ID gène: 10489