TTR anticorps

N° du produit ABIN7101619

Détail du produit anti-TTR anticorps

Antigène: TTR (Transthyretin (TTR))

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp TTR est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée: Humain, Souris

Attributs du produit: Monoclonal Antibodies

Purification: Affinity purification

Immunogène: A synthesized peptide derived from human TTR

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur TTR

Antigène: TTR (Transthyretin (TTR))

Autre désignation: TTR (TTR Produits)

Synonymes: anticorps zgc:103583, anticorps TTR, anticorps LOC100226992, anticorps CTS, anticorps CTS1, anticorps HsT2651, anticorps PALB, anticorps TBPA, anticorps AA408768, anticorps AI787086, anticorps D17860, anticorps prealbumin, anticorps Lr1, anticorps Tbpa, anticorps Prealbumin, anticorps xTTR, anticorps transthyretin (prealbumin, amyloidosis type I), anticorps transthyretin, anticorps Transthyretin, anticorps transthyretin (prealbumin, amyloidosis type 1), anticorps transthyretin-like, anticorps transthyretin L homeolog, anticorps ttr, anticorps TTR, anticorps vpb38, anticorps MRAD2831_RS38185, anticorps Caci_4246, anticorps LOC100226992, anticorps Ttr, anticorps ttr.L

Sujet: This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein, it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported, most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc. [provided by RefSeq, Jan 2009],CTS, CTS1, HEL111, HsT2651, PALB, TBPA,Blood,Blood_Serum Proteins,Cardiovascular,Neurodegenerative Diseases,Neurodegenerative Diseases_Amyloid Plaque and Neurofibrillary Tangle Formation in Alzheimers Disease,Neuroscience,TTR

Poids moléculaire: 16 kDa

ID gène: 7276

UniProt: P02766

Pathways: Hormone Transport