Anti-MYH9 Antibody (CAB0173)
- SKU:
- CAB0173
- 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-MYH9 Antibody |
| 抗体コード: | CAB0173 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | WB IHC IP |
| 反応性: | Human, Mouse, Rat |
| 宿主種: | Rabbit |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1711-1960 of human MYH9 (NP_002464.1). |
| 申し込み: | WB IHC IP |
| 推奨希釈: | WB 1:1000 - 1:2000 IHC 1:50 - 1:100 IP 1:50 - 1:200 |
| 反応性: | Human, Mouse, Rat |
| ポジティブサンプル: | HeLa, Jurkat, LO2, SW480, Mouse liver, Mouse lung |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1711-1960 of human MYH9 (NP_002464.1). |
| 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: | ANSS GKGA LALE EKRR LEAR IAQL EEEL EEEQ GNTE LIND RLKK ANLQ IDQI NTDL NLER SHAQ KNEN ARQQ LERQ NKEL KVKL QEME GTVK SKYK ASIT ALEA KIAQ LEEQ LDNE TKER QAAC KQVR RTEK KLKD VLLQ VDDE RRNA EQYK DQAD KAST RLKQ LKRQ LEEA EEEA QRAN ASRR KLQR ELED ATET ADAM NREV SSLK NKLR RGDL PFVV PRRM ARKG AGDG SDEE VDGK ADGA EAKP AE |
| 遺伝子ID: | 4627 |
| Uniprot: | P35579 |
| セルラーロケーション: | Cytoplasm, cell cortex, cytoskeleton |
| 計算された分子量: | 159kDa/226kDa |
| 観察された分子量: | 250kDa |
| 同義語: | MYH9, BDPLT6, DFNA17, EPSTS, FTNS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA, myosin-9 |
| バックグラウンド: | This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. |
| UniProt Protein Function: | MYH9: Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. Interacts with PDLIM2. Interacts with SLC6A4. Myosin is a hexameric protein that consists of 2 heavy chain subunits (MHC), 2 alkali light chain subunits (MLC) and 2 regulatory light chain subunits (MLC-2). Interacts with RASIP1. Interacts with DDR1. Interacts with SVIL and HTRA3. In the kidney, expressed in the glomeruli. Also expressed in leukocytes. 2 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Motor; Motility/polarity/chemotaxis; Actin-binding Chromosomal Location of Human Ortholog: 22q13.1 Cellular Component: actin cytoskeleton; actomyosin; cleavage furrow; contractile ring; cytoplasm; cytosol; focal adhesion; immunological synapse; integrin complex; leading edge; membrane; myosin II complex; nucleus; plasma membrane; protein complex; ruffle; signalosome; stress fiber; uropod Molecular Function:actin binding; actin filament binding; actin-dependent ATPase activity; ADP binding; ATP binding; ATPase activity; microfilament motor activity; protein anchor; protein binding; protein domain specific binding; protein homodimerization activity Biological Process: actin cytoskeleton reorganization; actin filament-based movement; actomyosin structure organization and biogenesis; angiogenesis; blood vessel endothelial cell migration; cytokinesis; membrane protein ectodomain proteolysis; monocyte differentiation; phagocytosis, engulfment; platelet formation; protein transport; regulation of cell shape Disease: Deafness, Autosomal Dominant 17; Epstein Syndrome; Fechtner Syndrome; Macrothrombocytopenia And Progressive Sensorineural Deafness; May-hegglin Anomaly; Sebastian Syndrome |
| NCBI Summary: | This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011] |
| UniProt Code: | P35579 |
| NCBI GenInfo Identifier: | 6166599 |
| NCBI Gene ID: | 4627 |
| NCBI Accession: | P35579.4 |
| UniProt Secondary Accession: | P35579,O60805, Q60FE2, Q86T83, A8K6E4, |
| UniProt Related Accession: | P35579 |
| Molecular Weight: | 159,864 Da |
| NCBI Full Name: | Myosin-9 |
| NCBI Synonym Full Names: | myosin, heavy chain 9, non-muscle |
| NCBI Official Symbol: | MYH9 |
| NCBI Official Synonym Symbols: | MHA; FTNS; EPSTS; BDPLT6; DFNA17; NMMHCA; NMHC-II-A; NMMHC-IIA |
| NCBI Protein Information: | myosin-9 |
| UniProt Protein Name: | Myosin-9 |
| UniProt Synonym Protein Names: | Cellular myosin heavy chain, type A; Myosin heavy chain 9; Myosin heavy chain, non-muscle IIa; Non-muscle myosin heavy chain A; NMMHC-A; Non-muscle myosin heavy chain IIa; NMMHC II-a; NMMHC-IIA |
| Protein Family: | Myosin |
| UniProt Gene Name: | MYH9 |
| UniProt Entry Name: | MYH9_HUMAN |
 | Western blot analysis of extracts of various cell lines, using MYH9 antibody (CAB0173) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 15s. |
 | Immunohistochemistry of paraffin-embedded human esophagus using MYH9 antibody (CAB0173) at dilution of 1:100 (40x lens). |
 | Immunohistochemistry of paraffin-embedded human stomach using MYH9 antibody (CAB0173) at dilution of 1:100 (40x lens). |
 | Immunoprecipitation analysis of 300ug extracts of HeLa cells using 3ug MYH9 antibody (CAB0173). Western blot was performed from the immunoprecipitate using MYH9 antibody (CAB0173) at a dilition of 1:1000. |
View AllClose