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Invitrogen™ DLX5 Polyclonal Antibody

Description
Immunogen sequence: RRVPSIRSGD FQAPFQTSAA MHHPSQESPT LPESSATDSD YYSPTGGAPH GYCSPTSASY GKALNPYQYQ YHGVNGSAGS YPAKAYADYS YASSYHQYGG AYNRVPSATN QPEKEVTEPE VRMVNGKPKK VRKP Highest antigen sequence indentity to the following orthologs: Mouse - 93%, Rat - 92%.
This gene encodes a member of a homeobox transcription factor gene family similar 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.
Specifications
Specifications
| Antigen | DLX5 |
| Applications | Immunohistochemistry (Paraffin), Immunocytochemistry |
| Classification | Polyclonal |
| Concentration | 0.2 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 |
| Gene | DLX5 |
| Gene Accession No. | P56178 |
| Gene Alias | AI385752; distal-less homeo box 5; distal-less homeobox 5; distal-less homeobox protein 5; DLX-3; DLX5; Homeobox protein DLX-3; homeobox protein DLX-5; RDLX; SHFM1D; split hand/foot malformation type 1 with sensorineural hearing loss; Unknown (protein for MGC:137934) |
| Gene Symbols | DLX5 |
| Show More |
Product Title
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