SLC16A2/MCT8 anticorps (AA 112-161)

N° du produit ABIN1451355

Cet anticorps anti-SLC16A2/MCT8 Polyclonal Lapin (ABIN1451355) détecte spécifiquement SLC16A2/MCT8 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour SLC16A2/MCT8 anticorps (AA 112-161) (ABIN1451355)

Antigène: SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC16A2/MCT8 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-SLC16A2/MCT8 anticorps

Épitope: AA 112-161

Fonction: MCT8 Antibody

Specificité: MCT8 Polyclonal Antibody detects endogenous levels of MCT8 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: The antiserum was produced against synthesized peptide derived from human SLC16A2. AA range:112-161

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. ELISA: 1:40000. Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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/1 year

Date de péremption: 12 months

Détails sur SLC16A2/MCT8

Antigène: SLC16A2/MCT8 (SLC16A2) (Solute Carrier Family 16 Member 2 (SLC16A2))

Autre désignation: SLC16A2

Sujet:

Synonyms: SLC16A2, MCT8, XPCT, Monocarboxylate transporter 8, MCT 8, Monocarboxylate transporter 7, MCT 7, Solute carrier family 16 member 2, X-linked PEST-containing transporter

Background: This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq, Mar 2012],

Gene Name: SLC16A2

Protein Name: Monocarboxylate transporter 8

Poids moléculaire: 59 kDa

ID gène: 6567

OMIM: 300095

UniProt: P36021

Pathways: Hormone Transport