FTSJ1 anticorps (AA 1-110) (Biotin)

N° du produit ABIN1701272

Détail du produit anti-FTSJ1 anticorps (Biotin)

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

Épitope: AA 1-110

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))

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 (FTSJ1 Produits)

Synonymes: anticorps AI931847, anticorps Ftsj, anticorps Ftsjl, anticorps Sfc12, anticorps CDLIV, anticorps MRX44, anticorps MRX9, anticorps SPB1, anticorps TRMT7, anticorps RGD1561061, anticorps FtsJ RNA methyltransferase homolog 1 (E. coli), anticorps FtsJ RNA methyltransferase homolog 1, anticorps Ftsj1, anticorps 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).