TMED6 anticorps (AA 125-153)

N° du produit ABIN5538213

L’anticorps anti-TMED6 Polyclonal Lapin est utilisé pour la détection de TMED6 dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour TMED6 anticorps (AA 125-153) (ABIN5538213)

Antigène: TMED6 (Transmembrane Emp24 Protein Transport Domain Containing 6 (TMED6))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMED6 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-TMED6 anticorps

Épitope: AA 125-153

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This TMED6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 125-153 amino acids from the Central region of human TMED6.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur TMED6

Antigène: TMED6 (Transmembrane Emp24 Protein Transport Domain Containing 6 (TMED6))

Autre désignation: TMED6

Sujet: TMED6 (transmembrane emp24 domain-containing protein 6) is a 240 amino acid single-pass type I membrane protein that belongs to the EMP24/GP25L family and contains one GOLD domain. The gene that encodes TMED6 contains around 8,564 bases and maps to human chromosome 16q22.1. Encoding over 900 genes and consisting of approximately 90 million base pairs, chromosome 16 makes up nearly 3 % of the human genome and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, when mutated, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. Alterations in the CREB gene and NOD2 gene, both of which are located on chromosome 16, result in Rubinstein-Taybi syndrome and Crohn's disease, respectively. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

Poids moléculaire: 28 kDa

ID gène: 146456

UniProt: Q8WW62