LURAP1L anticorps (Alexa Fluor 680)

N° du produit ABIN4998765

Détail du produit anti-LURAP1L anticorps (Alexa Fluor 680)

Antigène: LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LURAP1L est conjugé à/à la Alexa Fluor 680

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C9orf150

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 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 LURAP1L

Antigène: LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))

Autre désignation: C9orf150 (LURAP1L Produits)

Synonymes: anticorps C9orf150, anticorps bA3L8.2, anticorps RGD1308059, anticorps 1110029A09Rik, anticorps AV077978, anticorps AV175137, anticorps D4Bwg0951e, anticorps WI-13707, anticorps bM350F23.1, anticorps leucine rich adaptor protein 1 like, anticorps leucine rich adaptor protein 1-like, anticorps LURAP1L, anticorps Lurap1l

Sujet:

Synonyms: LURAP1L, bA3L8.2, FLJ38505, C9orf150, Chromosome 9 open reading frame 150, CI150_HUMAN, FLJ90271, HYST0841, MGC46502, Uncharacterized protein C9orf150.

Background: C9orf150 is a 231 amino acid protein encoded by a gene that maps to human chromosome 9p23. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

ID gène: 286343