KIAA1522 anticorps (AA 101-250)

N° du produit ABIN1387607

Détail du produit anti-KIAA1522 anticorps

Antigène: KIAA1522

Épitope: AA 101-250

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KIAA1522 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Réactivité croisée: Humain

Homologie: Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human KIAA1522

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Références pour anticorps anti-KIAA1522 (ABIN1387607)

Liu, Yang, Cao, Jiang, Hao, Xu, Cai, Wang: "KIAA1522 is a novel prognostic biomarker in patients with non-small cell lung cancer." dans: Scientific reports, Vol. 6, pp. 24786, (2017) (PubMed).

Détails sur KIAA1522

Antigène: KIAA1522

Autre désignation: KIAA1522 (KIAA1522 Produits)

Synonymes: anticorps Kiaa1522, anticorps mKIAA1522, anticorps expressed sequence C77080, anticorps KIAA1522, anticorps KIAA1522 ortholog, anticorps C77080, anticorps KIAA1522

Sujet:

Synonyms: K1522_HUMAN, Kiaa1522, Uncharacterized protein KIAA1522.

Background: KIAA1522 is a 1,035 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 1p35.1. Chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

ID gène: 57648