TSPEAR Antibody (PACO15728)
- SKU:
- PACO15728
- Product Type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Applications:
- ELISA
- Applications:
- IHC
- Antibody Type:
- Polyclonal Antibody
- Conjugation:
- Unconjugated
Description
| Antibody Name: | TSPEAR Antibody (PACO15728) |
| Antibody SKU: | PACO15728 |
| Size: | 50ul |
| Host Species: | Rabbit |
| Tested Applications: | ELISA, IHC |
| Recommended Dilutions: | ELISA:1:1000-1:5000, IHC:1:50-1:200 |
| Species Reactivity: | Human |
| Immunogen: | Fusion protein of human TSPEAR |
| Form: | Liquid |
| Storage Buffer: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Purification Method: | Antigen affinity purification |
| Clonality: | Polyclonal |
| Isotype: | IgG |
| Conjugate: | Non-conjugated |
 | The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using PACO15728(TSPEAR Antibody) at dilution 1/50, on the right is treated with fusion protein. (Original magnification: x200). |
 | The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using PACO15728(TSPEAR Antibody) at dilution 1/50, on the right is treated with fusion protein. (Original magnification: x200). |
| Background: | This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. |
| Synonyms: | thrombospondin-type laminin G domain and EAR repeats |
| UniProt Protein Function: | TSPEAR: 2 isoforms of the human protein are produced by alternative splicing.Protein type: Secreted, signal peptide; SecretedChromosomal Location of Human Ortholog: 21q22.3Cellular Component: cell surface; stereociliumBiological Process: sensory perception of soundDisease: Deafness, Autosomal Recessive 98 |
| UniProt Protein Details: | |
| NCBI Summary: | This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] |
| UniProt Code: | Q8WU66 |
| NCBI GenInfo Identifier: | 26006900 |
| NCBI Gene ID: | 54084 |
| NCBI Accession: | Q8WU66.2 |
| UniProt Secondary Accession: | Q8WU66 |
| UniProt Related Accession: | Q8WU66 |
| Molecular Weight: | 66,722 Da |
| NCBI Full Name: | Thrombospondin-type laminin G domain and EAR repeat-containing protein |
| NCBI Synonym Full Names: | thrombospondin type laminin G domain and EAR repeats |
| NCBI Official Symbol: | TSPEAR |
| NCBI Official Synonym Symbols: | DFNB98; TSP-EAR; C21orf29 |
| NCBI Protein Information: | thrombospondin-type laminin G domain and EAR repeat-containing protein |
| UniProt Protein Name: | Thrombospondin-type laminin G domain and EAR repeat-containing protein |
| UniProt Synonym Protein Names: | |
| Protein Family: | Thrombospondin-type laminin G domain and EAR repeat-containing protein |
| UniProt Gene Name: | TSPEAR |
| UniProt Entry Name: | TSEAR_HUMAN |
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