DEXI anticorps (AA 51-95) (Biotin)
-
- Antigène Voir toutes DEXI Anticorps
- DEXI (Dexamethasone-Induced Transcript (DEXI))
-
Épitope
- AA 51-95
-
Reactivité
- Souris
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp DEXI est conjugé à/à la Biotin
-
Application
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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
- Top Product
- Discover our top product DEXI Anticorps primaire
-
-
- Indications d'application
-
IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
-
- 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
-
- 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
-