SMPX Antibody (PACO44306)
- SKU:
- PACO44306
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- IHC
- Application:
- IF
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | SMPX Antibody (PACO44306) |
抗体コード: | PACO44306 |
サイズ: | 50ul |
宿主種: | Rabbit |
申し込み: | ELISA, IHC, IF |
推奨される希釈: | ELISA:1:2000-1:10000, IHC:1:20-1:200, IF:1:50-1:200 |
反応性: | Human |
免疫原: | Recombinant Human Small muscular protein (1-88AA) |
憲法: | Liquid |
ストレージバッファ: | PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
精製方法: | Antigen Affinity Purified |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
![]() | Immunohistochemistry of paraffin-embedded human kidney tissue using PACO44306 at dilution of 1:100. |
![]() | Immunofluorescent analysis of HepG2 cells using PACO44306 at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L). |
![]() | Immunohistochemistry of paraffin-embedded human heart tissue using PACO44306 at dilution of 1:100. |
バックグラウンド: | Plays a role in the regulatory network through which muscle cells coordinate their structural and functional states during growth, adaptation, and repair. |
シノニム: | Small muscular protein (Stretch-responsive skeletal muscle protein), SMPX, SRMX |
UniProt Protein Function: | SMPX: Plays a role in the regulatory network through which muscle cells coordinate their structural and functional states during growth, adaptation, and repair. Defects in SMPX are the cause of deafness X-linked type 4 (DFNX4). A non-syndromic form of sensorineural, progressive hearing loss with postlingual onset. In affected males, the auditory impairment affects initially high-frequency hearing. It later evolves to become severe to profound and affects all frequencies. Carrier females manifest moderate hearing impairment in the high frequencies. Belongs to the SMPX family. |
UniProt Protein Details: | Protein type:Motility/polarity/chemotaxis Chromosomal Location of Human Ortholog: Xp22.1 Cellular Component: muscle tendon junction; costamere; M band; nucleus Biological Process: striated muscle contraction Disease: Deafness, X-linked 4 |
NCBI Summary: | This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011] |
UniProt Code: | Q9UHP9 |
NCBI GenInfo Identifier: | 239938852 |
NCBI Gene ID: | 23676 |
NCBI Accession: | Q9UHP9.3 |
UniProt Secondary Accession: | Q9UHP9,B1AWX2, |
UniProt Related Accession: | Q9UHP9 |
Molecular Weight: | 88 |
NCBI Full Name: | Small muscular protein |
NCBI Synonym Full Names: | small muscle protein, X-linked |
NCBI Official Symbol: | SMPX |
NCBI Official Synonym Symbols: | DFN6; DFNX4 |
NCBI Protein Information: | small muscular protein; deafness, X-linked 6, sensorineural; stretch-responsive skeletal muscle protein |
UniProt Protein Name: | Small muscular protein |
UniProt Synonym Protein Names: | Stretch-responsive skeletal muscle protein |
Protein Family: | Small muscular protein |
UniProt Gene Name: | SMPX |
UniProt Entry Name: | SMPX_HUMAN |