DEXI antibody (AA 51-95) (AbBy Fluor® 647)
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- Target See all DEXI Antibodies
- DEXI (Dexamethasone-Induced Transcript (DEXI))
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Binding Specificity
- AA 51-95
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Reactivity
- Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This DEXI antibody is conjugated to AbBy Fluor® 647
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Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 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
- Top Product
- Discover our top product DEXI Primary Antibody
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- Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- 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
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- Target
- DEXI (Dexamethasone-Induced Transcript (DEXI))
- Alternative Name
- DEXI (DEXI Products)
- Synonyms
- 1810029J14Rik antibody, AI836170 antibody, AW413143 antibody, D16Bwg0586e antibody, Myle antibody, MYLE antibody, RGD1564938 antibody, zgc:101082 antibody, dexamethasone-induced transcript antibody, Dexi homolog antibody, Dexi homolog (mouse) antibody, Dexi antibody, DEXI antibody, dexi antibody
- Background
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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
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