Cell Biology Antibodies 5
Anti-DLX5 Antibody (CAB15049)
- SKU:
- CAB15049
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Description
Antibody Name: | Anti-DLX5 Antibody |
Antibody SKU: | CAB15049 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 200 to the C-terminus of human DLX5 (NP_005212.1). |
Application: | WB |
Recommended Dilution: | WB 1:500 - 1:2000 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | 293T, HeLa, mouse brain, rat brain |
Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 200 to the C-terminus of human DLX5 (NP_005212.1). |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | EMPP EHSP SSSD PMAC NSPQ SPAV WEPQ GSSR SLSH HPHA HPPT SNQS PASS YLEN SASW YTSA ASSI NSHL PPPG SLQH PLAL ASGT LY |
Gene ID: | 1749 |
Uniprot: | P56178 |
Cellular Location: | Nucleus |
Calculated MW: | 20kDa/31kDa |
Observed MW: | 36kDa |
Synonyms: | DLX5, SHFM1D |
Background: | 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. |
UniProt Protein Function: | DLX5: Transcriptional factor involved in bone development. Acts as an immediate early BMP-responsive transcriptional activator essential for osteoblast differentiation. Stimulates ALPL promoter activity in a RUNX2-independent manner during osteoblast differentiation. Stimulates SP7 promoter activity during osteoblast differentiation. Promotes cell proliferation by up-regulating MYC promoter activity. Involved as a positive regulator of both chondrogenesis and chondrocyte hypertrophy in the endochondral skeleton. Binds to the homeodomain-response element of the ALPL and SP7 promoter. Binds to the MYC promoter. Requires the 5'-TAATTA-3' consensus sequence for DNA-binding. Defects in DLX5 are the cause of split-hand/foot malformation type 1, with sensorineural hearing loss (SHFM1D). A disease characterized by the association of split- hand/foot malformation with deafness. Split-hand/foot malformation is a limb malformation involving the central rays of the autopod and presenting with syndactyly, median clefts of the hands and feet, and aplasia and/or hypoplasia of the phalanges, metacarpals, and metatarsals. Some patients have been found to have mental retardation, ectodermal and craniofacial findings, and orofacial clefting. Belongs to the distal-less homeobox family. |
UniProt Protein Details: | Protein type:Transcription factor; DNA-binding Chromosomal Location of Human Ortholog: 7q22 Cellular Component: nuclear chromatin Biological Process: BMP signaling pathway; cell proliferation; endochondral ossification; nervous system development; osteoblast differentiation; positive regulation of transcription, DNA-dependent; skeletal development Disease: Split-hand/foot Malformation 1 With Sensorineural Hearing Loss, Autosomal Recessive |
NCBI Summary: | 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. [provided by RefSeq, Jul 2008] |
UniProt Code: | P56178 |
NCBI GenInfo Identifier: | 12644329 |
NCBI Gene ID: | 1749 |
NCBI Accession: | P56178.2 |
UniProt Secondary Accession: | P56178,Q9UPL1, B7Z4P3, |
UniProt Related Accession: | P56178 |
Molecular Weight: | 20,900 Da |
NCBI Full Name: | Homeobox protein DLX-5 |
NCBI Synonym Full Names: | distal-less homeobox 5 |
NCBI Official Symbol: | DLX5 |
NCBI Official Synonym Symbols: | SHFM1D |
NCBI Protein Information: | homeobox protein DLX-5 |
UniProt Protein Name: | Homeobox protein DLX-5 |
Protein Family: | Homeobox protein |
UniProt Gene Name: | DLX5 |
UniProt Entry Name: | DLX5_HUMAN |
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