RIMKLA anticorps (Cy3)

N° du produit ABIN1421765

Détail du produit anti-RIMKLA anticorps (Cy3)

Antigène: RIMKLA (Ribosomal Modification Protein RimK-Like Family Member A (RIMKLA))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RIMKLA est conjugé à/à la Cy3

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 RIMKLA/FAM80A

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 RIMKLA

Antigène: RIMKLA (Ribosomal Modification Protein RimK-Like Family Member A (RIMKLA))

Autre désignation: RIMKLA (RIMKLA Produits)

Synonymes: anticorps FAM80A, anticorps NAAGS, anticorps NAAGS-II, anticorps B930030J24, anticorps Rimk, anticorps RGD1306880, anticorps ribosomal modification protein rimK like family member A, anticorps ribosomal modification protein rimK-like family member A, anticorps RIMKLA, anticorps Rimkla

Sujet:

Synonyms: Family with sequence similarity 80, member A, MGC47816, Ribosomal protein S6 modication like protein A, RIMKLA, RIMKA_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. The FAM80A gene product has been provisionally designated FAM80A pending further characterization.