Aristaless Related Homeobox (ARX) (Middle Region) Peptid
ARX
Reaktivität: Human
Wirt: Synthetic
BP, WB
Produktnummer ABIN973474
150,78 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach:
Deutschland
Lieferung in 15 bis 22 Werktagen
Kurzübersicht für Aristaless Related Homeobox (ARX) (Middle Region) Peptid (ABIN973474)
Target
Arx (ARX)
(Aristaless Related Homeobox (ARX))
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- Middle Region
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Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-ARX antibody (Catalog #: ARP31598_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
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Aufreinigung
- Purified
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Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Konzentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Handhabung
- Avoid repeated freeze-thaw cycles.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Arx (ARX) (Aristaless Related Homeobox (ARX))
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Hintergrund
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ARX gene is a homeobox-containing gene expressed during development. The expressed protein ARX contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Mutations in this gene cause X-linked mental retardation and epilepsy.This gene is a homeobox-containing gene expressed during development. The expressed protein contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Mutations in this gene cause X-linked mental retardation and epilepsy. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRXS1, PRTS, CT121, EIEE1, MRX76, MRX87
Protein Size: 562 -
Molekulargewicht
- 58 kDa
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Gen-ID
- 170302
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NCBI Accession
- NM_139058, NP_620689
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UniProt
- Q96QS3
Target
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