FTSJ1 anticorps (AA 1-110) (Biotin)

N° du produit ABIN1701272

L’anticorps Lapin Polyclonal anti-FTSJ1 a été validé pour ELISA, IHC (fro) et IHC (p). Il convient pour détecter FTSJ1 dans des échantillons de Souris et Rat.

Aperçu rapide pour FTSJ1 anticorps (AA 1-110) (Biotin) (ABIN1701272)

Antigène: FTSJ1 (FtsJ RNA Methyltransferase Homolog 1 (FTSJ1))

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FTSJ1 est conjugé à/à la Biotin

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

Détail du produit anti-FTSJ1 anticorps (Biotin)

Épitope: AA 1-110

Réactivité croisée: Souris, Rat

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

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FTSJ1

Isotype: IgG

Information d'application

Indications d'application: 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 FTSJ1

Antigène: FTSJ1 (FtsJ RNA Methyltransferase Homolog 1 (FTSJ1))

Autre désignation: FTSJ1

Sujet:

Synonyms: CDLIV, FTSJ 1, FtsJ homolog 1 E. coli, FtsJ homolog 1, JM23, Mental retardation X linked 44, Mental retardation X linked 9, MRX44, MRX9, Putative ribosomal RNA methyltransferase 1, RRMJ1, SPB1, TRM7, RRMJ1_HUMAN.

Background: FTSJ1 is a 329 amino acid nucleolar protein belonging to the RlmE family and methyltransferase superfamily. Expressed in adult thalamus, hippocampus, amygdala, corpus callosum and caudate nucleus, as well as fetal kidney, lung, liver, brain and lung, FTSJ1 plays a role in rRNA modification and processing. FTSJ1 exists as multiple spliced isoforms which are encoded by a gene located on human chromosome Xp11.23. Notably, defects in the gene encoding FTSJ1 are the cause of mental retardation X-linked type 44 (MRX44) and nonsyndromic X-linked mental retardation (MRX9).