Anti-DSP Antibody (CAB17477)
- SKU:
- CAB17477
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
| Antibody Name: | Anti-DSP Antibody |
| Antibody SKU: | CAB17477 |
| Antibody Size: | 20uL, 50 uL |
| Application: | WB IF |
| Reactivity: | Human, Mouse |
| Host Species: | Rabbit |
| Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 1-100 of human DSP (NP_004406.2). |
| Application: | WB IF |
| Recommended Dilution: | WB 1:500 - 1:2000 IF 1:50 - 1:200 |
| Reactivity: | Human, Mouse |
| Positive Samples: |
| Immunogen: | A synthetic peptide corresponding to a sequence within amino acids 1-100 of human DSP (NP_004406.2). |
| 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: | MSCN GGSH PRIN TLGR MIRA ESGP DLRY EVTS GGGG TSRM YYSR RGVI TDQN SDGY CQTG TMSR HQNQ NTIQ ELLQ NCSD CLMR AELI VQPE LKYG DGIQ |
| Gene ID: | 1832 |
| Uniprot: | P15924 |
| Cellular Location: | |
| Calculated MW: | 260kDa/278kDa/331kDa |
| Observed MW: | Refer to figures |
| Synonyms: | DCWHKTA, DP, DSP |
| Background: | This gene encodes a protein that anchors intermediate filaments to desmosomal plaques and forms an obligate component of functional desmosomes. Mutations in this gene are the cause of several cardiomyopathies and keratodermas, including skin fragility-woolly hair syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016] |
| UniProt Protein Function: | Desmoplakin: Major high molecular weight protein of desmosomes. Involved in the organization of the desmosomal cadherin- plakoglobin complexes into discrete plasma membrane domains and in the anchoring of intermediate filaments to the desmosomes. Homodimer. Interacts with COL17A1 (via cytoplasmic region). Associates (via C-terminal) with KRT5-KRT14 (via rod region), KRT8-KRT18 and VIM intermediate filaments. Interacts with DSC2. Isoform DPI is apparently an obligate constituent of all desmosomes. Isoform DPII resides predominantly in tissues and cells of stratified origin. Belongs to the plakin or cytolinker family. 2 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis; Cytoskeletal; Cell adhesion Chromosomal Location of Human Ortholog: 6p24 Cellular Component: desmosome; mitochondrion; basolateral plasma membrane; plasma membrane; intermediate filament; cornified envelope; fascia adherens; nucleus Molecular Function:protein binding, bridging; protein binding; protein kinase C binding; structural constituent of cytoskeleton; cell adhesion molecule binding; structural molecule activity Biological Process: keratinocyte differentiation; cell-cell adhesion; epidermis development; wound healing; apoptosis; intermediate filament organization; peptide cross-linking; cell structure disassembly during apoptosis Disease: Cardiomyopathy, Dilated, With Woolly Hair And Keratoderma; Arrhythmogenic Right Ventricular Dysplasia, Familial, 8; Keratosis Palmoplantaris Striata Ii; Cardiomyopathy, Dilated, With Woolly Hair, Keratoderma, And Tooth Agenesis; Skin Fragility-woolly Hair Syndrome; Epidermolysis Bullosa, Lethal Acantholytic |
| NCBI Summary: | Desmosomes are intercellular junctions that tightly link adjacent cells. Desmoplakin is an obligate component of functional desmosomes that anchors intermediate filaments to desmosomal plaques. The N-terminus of desmoplakin is required for localization to the desmosome and interacts with the N-terminal region of plakophilin 1 and plakoglobin. The C-terminus of desmoplakin binds with intermediate filaments. In the mid-region of desmoplakin, a coiled-coiled rod domain is responsible for homodimerization. Mutations in this gene are the cause of several cardiomyopathies and keratodermas as well as the autoimmune disease paraneoplastic pemphigus. [provided by RefSeq, Jul 2008] |
| UniProt Code: | P15924 |
| NCBI GenInfo Identifier: | 58530840 |
| NCBI Gene ID: | 1832 |
| NCBI Accession: | NP_004406.2 |
| UniProt Secondary Accession: | P15924,O75993, Q14189, Q9UHN4, B2RTT2, D7RX09, |
| UniProt Related Accession: | P15924 |
| Molecular Weight: | 278,916 Da |
| NCBI Full Name: | desmoplakin isoform I |
| NCBI Synonym Full Names: | desmoplakin |
| NCBI Official Symbol: | DSPÂ Â |
| NCBI Official Synonym Symbols: | DP; DPI; DPII; DCWHKTAÂ Â |
| NCBI Protein Information: | desmoplakin |
| UniProt Protein Name: | Desmoplakin |
| UniProt Synonym Protein Names: | 250/210 kDa paraneoplastic pemphigus antigen |
| Protein Family: | Desmoplakin |
| UniProt Gene Name: | DSPÂ Â |
| UniProt Entry Name: | DESP_HUMAN |
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