EGR2 anticorps (Internal Region)
Aperçu rapide pour EGR2 anticorps (Internal Region) (ABIN375194)
Antigène
Voir toutes EGR2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Internal Region
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Séquence
- HGTAGPDRKP FPC
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Specificité
- This antibody recognizes EGR2
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Réactivité croisée (Details)
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Species reactivity (expected):Mouse, Rat and Canine.
Species reactivity (tested):Human. -
Purification
- Ammonium sulphate precipitation followed by antigen Affinity Chromatography using the immunizing peptide.
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Immunogène
- Peptide with sequence from the internal region of the protein sequence according to NP_000390.2. Genename: EGR2
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Indications d'application
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Peptide ELISA: Detection Limit: 1/64000. Western blot: 0.03-0.1 μg/mL. Approx 55 kDa band observed in lysates of cell line HepG2(calculated MW of 50.5 kDa according to NP_000390.2). Immunohistochemistry: 3-5 μg/mL. In paraffin embedded Human Colon shows nuclearstaining of absorptive cells.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. -
Restrictions
- For Research Use only
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Concentration
- 0.5 mg/mL
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Buffer
- Tris saline, pH 7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- Avoid repeated freezing and thawing.
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Stock
- 4 °C/-20 °C
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Stockage commentaire
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- EGR2 (Early Growth Response 2 (EGR2))
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Autre désignation
- EGR2
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Sujet
- ERG2 is a sequence-specific transcription factor, that binds to two specific DNA sites located in the promoter region of HOXA4. Defects in EGR2 are a cause of congenital hypomyelination neuropathy (CHN), which can be inherited in either an autosomal dominant or recessive manner. Recessive CHN can present as Charcot-Marie-Tooth disease type 4E, type 1D, or Dejerine-Sottas syndrome (DSS), a group of neuropathies associated with decreased nerve conduction velocities.Synonyms: AT591, EGR-2, Early growth response protein 2, KROX20, Krox 20, Zinc finger protein Krox-20
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ID gène
- 1959
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NCBI Accession
- NP_000390
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UniProt
- P11161
Antigène
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