Distal-Less Homeobox 5 (DLX5) Peptid
DLX5
Reaktivität: Human
Wirt: Synthetic
BP, IHC, WB
Produktnummer ABIN975855
150,78 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach:
Deutschland
Lieferung in 15 bis 22 Werktagen
Kurzübersicht für Distal-Less Homeobox 5 (DLX5) Peptid (ABIN975855)
Target
DLX5
(Distal-Less Homeobox 5 (DLX5))
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
-
-
Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-DLX5 antibody (Catalog #: ARP38586_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.
-
Aufreinigung
- Purified
-
-
Distal-Less Homeobox 5 (DLX5) peptide
DLX5 Reaktivität: Human, Maus, Ratte, Rind (Kuh) Wirt: Synthetic BP, Imm
-
-
Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
-
Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
-
-
Format
- Lyophilized
-
Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
-
Konzentration
- 1 mg/mL
-
Buffer
- Final peptide concentration is 1 mg/mL in PBS.
-
Handhabung
- Avoid repeated freeze-thaw cycles.
-
Lagerung
- -20 °C
-
Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
-
-
- DLX5 (Distal-Less Homeobox 5 (DLX5))
-
Hintergrund
-
DLX5 is a member of a homeobox transcription factor family. DLX5 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.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 -
Molekulargewicht
- 32 kDa
-
Gen-ID
- 1749
-
NCBI Accession
- NM_005221, NP_005212
-
UniProt
- P56178
Target
-
Sie sind hier:
