Aristaless Related Homeobox (ARX) (Middle Region) Peptide
ARX
Reactivity: Human
Host: Synthetic
BP, WB
Catalog No. ABIN973474
$160.46
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100 μg
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Quick Overview for Aristaless Related Homeobox (ARX) (Middle Region) Peptide (ABIN973474)
Target
Arx (ARX)
(Aristaless Related Homeobox (ARX))
Origin
Human
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- Middle Region
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Characteristics
- 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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Purification
- Purified
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Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- 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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Background
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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 -
Molecular Weight
- 58 kDa
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Gene ID
- 170302
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NCBI Accession
- NM_139058, NP_620689
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UniProt
- Q96QS3
Target
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