Anti-SMPX Antibody (CAB6744)
- SKU:
- CAB6744
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
抗体名: | Anti-SMPX Antibody |
抗体コード: | CAB6744 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IF |
反応性: | Human, Mouse, Rat |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-88 of human SMPX (NP_055147.1). |
申し込み: | WB IF |
推奨希釈: | WB 1:500 - 1:2000 IF 1:50 - 1:100 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | Mouse heart, Rat heart |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-88 of human SMPX (NP_055147.1). |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | MNMS KQPV SNVR AIQA NINI PMGA FRPG AGQP PRRK ECTP EVEE GVPP TSDE EKKP IPGA KKLP GPAV NLSE IQNI KSEL KYVP KAEQ |
遺伝子ID: | 23676 |
Uniprot: | Q9UHP9 |
セルラーロケーション: | |
計算された分子量: | 9kDa |
観察された分子量: | 13kDa |
同義語: | SMPX, DFN6, DFNX4 |
バックグラウンド: | 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. |
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 |
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