DEXI antibody (AA 51-95) (AbBy Fluor® 680)

Catalog No. ABIN6942886

The Rabbit Polyclonal anti-DEXI antibody has been validated for IF (cc) and IF (p). It is suitable to detect DEXI in samples from Mouse.

Quick Overview for DEXI antibody (AA 51-95) (AbBy Fluor® 680) (ABIN6942886)

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

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DEXI antibody is conjugated to AbBy Fluor® 680

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

Product Details anti-DEXI Antibody (AbBy Fluor® 680)

Binding Specificity: AA 51-95

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human DEXI

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for DEXI

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

Alternative Name: DEXI

Background:

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.

Gene ID: 28955

UniProt: O95424