Distal-Less Homeobox 5 (DLX5) Peptide
DLX5
Reactivity: Human
Host: Synthetic
BP, IHC, WB
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- Target See all DLX5 products
- DLX5 (Distal-Less Homeobox 5 (DLX5))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-DLX5 antibody (Catalog #: ARP38585_T100). 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.
- Purification
- Purified
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Distal-Less Homeobox 5 (DLX5) peptide
DLX5 Reactivity: Human, Mouse, Rat, Cow Host: Synthetic BP, Imm
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- DLX5 (Distal-Less Homeobox 5 (DLX5))
- Synonyms
- SHFM1D Peptide, AI385752 Peptide, RDLX Peptide, X-dll3 Peptide, dll3 Peptide, MGC69418 Peptide, DLX5 Peptide, dlx5 Peptide, dlx4 Peptide, zgc:101787 Peptide, distal-less homeobox 5 Peptide, distal-less homeobox 5 L homeolog Peptide, distal-less homeobox 2b Peptide, distal-less homeobox 5a Peptide, DLX5 Peptide, Dlx5 Peptide, dlx5.L Peptide, dlx5 Peptide, dlx2b Peptide, dlx5a Peptide
- Background
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DLX5 is a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. This protein may play a role in bone development and fracture healing. Mutation in its gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.
Alias Symbols: SHFM1D
Protein Interaction Partner: MAGED1,MSX2,NCOA2,SOX10,SOX8,SPEN,DLX2,DLX5,HOXC8,MSX1,MSX2
Protein Size: 289 - Molecular Weight
- 31 kDa
- Gene ID
- 1749
- NCBI Accession
- NM_005221, NP_005212
- UniProt
- P56178
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