MYH9 monoclonal antibody (M01), clone 3C7
产品名称: MYH9 monoclonal antibody (M01), clone 3C7
英文名称: MYH9 monoclonal antibody (M01), clone 3C7
产品编号: H00004627-M01
产品价格: null
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围:
亚诺法生技股份有限公司(Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Mouse monoclonal antibody raised against a partial recombinant MYH9.
- Immunogen:
- MYH9 (AAH11915, 131 a.a. ~ 220 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- RLKQLKRQLEEAEEEAQRANASRRKLQRELEDATETADAMNREVSSLKNKLRRGDLPFVVPRRMARKGAGDGSDEEVDGKADGAEAKPAE
- Host:
- Mouse
- Reactivity:
- Human, Mouse
- Isotype:
- IgG2b Kappa
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (35.64 KDa) .
- MSDS:
- Download
- Applications
- Western Blot (Cell lysate)
- MYH9 monoclonal antibody (M01), clone 3C7 Western Blot analysis of MYH9 expression in A-431 ( Cat # L015V1 ).
- Protocol Download
- Western Blot (Cell lysate)
- MYH9 monoclonal antibody (M01), clone 3C7. Western Blot analysis of MYH9 expression in NIH/3T3 ( Cat # L018V1 ).
- Protocol Download
- Western Blot (Recombinant protein)
- Protocol Download
- Immunofluorescence
- enlarge this image
- Immunofluorescence of monoclonal antibody to MYH9 on A-431 cell . [antibody concentration 10 ug/ml]
- Protocol Download
- Sandwich ELISA (Recombinant protein)
- Detection limit for recombinant GST tagged MYH9 is 0.1 ng/ml as a capture antibody.
- Protocol Download
- Entrez GeneID:
- 4627
- GeneBank Accession#:
- BC011915
- Protein Accession#:
- AAH11915
- Gene Name:
- MYH9
- Gene Alias:
- DFNA17,EPSTS,FTNS,MGC104539,MHA,NMHC-II-A,NMMHCA
- Gene Description:
- myosin, heavy chain 9, non-muscle
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of 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
- Other Designations:
- MYH9 variant protein,OTTHUMP00000028706,cellular myosin heavy chain, type A,myosin, heavy polypeptide 9, non-muscle,non-muscle myosin heavy chain,non-muscle myosin heavy polypeptide 9,nonmuscle myosin heavy chain II-A
- Gene Pathway
- Related Disease
- Albuminuria
- Attention
- Bernard-Soulier Syndrome
- Blood Platelet Disorders
- Cardiovascular Diseases
- Cerebral Hemorrhage
- Chronic Disease
- Cleft Lip
- Cleft Palate
- Deafness
- Deafness
- Diabetes Mellitus
- Endocrine System Diseases
- Genetic Predisposition to Disease
- Glomerulonephritis
- Glomerulosclerosis, Focal Segmental
- Hypertension
- Intracranial Hemorrhages
- Kidney Diseases