LMOD3 Antibody (PACO10273)
- SKU:
- PACO10273
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | LMOD3 Antibody (PACO10273) |
抗体コード: | PACO10273 |
サイズ: | 50ul |
宿主種: | Rabbit |
申し込み: | ELISA, WB |
推奨される希釈: | |
反応性: | Human, Mouse, Rat |
免疫原: | Human LMOD3 |
憲法: | Liquid |
ストレージバッファ: | PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles. |
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 |
シノニム: | leiomodin 3 (fetal);LMOD3;DKFZp313F0135 ; |
UniProt Protein Function: | LMOD3: Belongs to the tropomodulin family. 2 isoforms of the human protein are produced by alternative splicing.Chromosomal Location of Human Ortholog: 3p14.1Cellular Component: striated muscle thin filamentMolecular Function: tropomyosin bindingBiological Process: actin filament organization; muscle contraction; myofibril assemblyDisease: Nemaline Myopathy 10 |
UniProt Protein Details: | |
NCBI Summary: | The protein encoded by this gene is a member of the leiomodin family of proteins. This protein contains three actin-binding domains, a tropomyosin domain, a leucine-rich repeat domain, and a Wiskott-Aldrich syndrome protein homology 2 domain (WH2). Localization of this protein to the pointed ends of thin filaments has been observed, and there is evidence that this protein acts as a catalyst of actin nucleation, and is important to the organization of sarcomeric thin filaments in skeletal muscles. Mutations in this gene have been associated as one cause of Nemaline myopathy, as other genes have also been linked to this disorder. Nemaline myopathy is a disorder characterized by nonprogressive generalized muscle weakness and protein inclusions (nemaline bodies) in skeletal myofibers. Patients with mutations in this gene often present with a severe congenital form of the disorder. [provided by RefSeq, Jan 2015] |
UniProt Code: | Q0VAK6 |
NCBI GenInfo Identifier: | 115528526 |
NCBI Gene ID: | 56203 |
NCBI Accession: | BC121019 |
UniProt Secondary Accession: | Q0VAK6,Q0JTT2, Q5JPG6, Q8IUK4, Q96LS4, B4DT85 |
UniProt Related Accession: | Q0VAK6 |
Molecular Weight: | 40,194 Da |
NCBI Full Name: | Homo sapiens leiomodin 3 (fetal), mRNA |
NCBI Synonym Full Names: | leiomodin 3 |
NCBI Official Symbol: | LMOD3 |
NCBI Official Synonym Symbols: | NEM10 |
NCBI Protein Information: | leiomodin-3 |
UniProt Protein Name: | Leiomodin-3 |
UniProt Synonym Protein Names: | Leiomodin, fetal form |
Protein Family: | Leiomodin |
UniProt Gene Name: | LMOD3 |
UniProt Entry Name: | LMOD3_HUMAN |