DEXI anticorps (AA 51-95) (Cy7)

N° du produit ABIN6942891

Détail du produit anti-DEXI anticorps (Cy7)

Antigène: DEXI (Dexamethasone-Induced Transcript (DEXI))

Épitope: AA 51-95

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DEXI est conjugé à/à la Cy7

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Souris

Homologie: Human,Rat,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human DEXI

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur DEXI

Antigène: DEXI (Dexamethasone-Induced Transcript (DEXI))

Autre désignation: DEXI (DEXI Produits)

Synonymes: anticorps 1810029J14Rik, anticorps AI836170, anticorps AW413143, anticorps D16Bwg0586e, anticorps Myle, anticorps MYLE, anticorps RGD1564938, anticorps zgc:101082, anticorps dexamethasone-induced transcript, anticorps Dexi homolog, anticorps Dexi homolog (mouse), anticorps Dexi, anticorps DEXI, anticorps dexi

Sujet:

Synonyms: Dexamethasone-induced protein, DEXI, DEXI_HUMAN, MYLE, Protein MYLE.

Background: DEXI is a 95 amino acid protein belonging to the DEXI family. Induced by dexamethasone, DEXI is expressed in brain, liver, pancreas, placenta and lung, with highest levels in heart. DEXI is also up-regulated in emphysematous lung compared to normal lung. The gene encoding DEXI maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition.

ID gène: 28955

UniProt: O95424