MYO5A polyclonal antibody
产品名称： MYO5A polyclonal antibody
英文名称： MYO5A polyclonal antibody
产品编号： PAB19013
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:
- Goat polyclonal antibody raised against synthetic peptide of MYO5A.
- Immunogen:
- A synthetic peptide corresponding to amino acids at internal region of human MYO5A.
- Sequence:
- C-ETKQLELDLN
- Host:
- Goat
- Theoretical MW (kDa):
- 200
- Reactivity:
- Human, Mouse
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In Tris saline, pH7.3 (0.5% BSA, 0.02% sodium azide)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- ELISA (1:8000)
Western Blot (1-3 ug/mL)
Immunofluorescence (1-3 ug/mL)
The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Applications
- Western Blot (Cell lysate)
- MYO5A polyclonal antibody (Cat # PAB19013) (1 ug/mL) staining of Jurkat lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
- Immunofluorescence
- MYO5A polyclonal antibody (Cat # PAB19013) (1 ug/mL) staining of Mouse Skeletal Muscle (first panel, and in green in third panel). Alpha-bungaratoxin staining in middle panel and in red in third panel. Detected by Fluorescence. Data kindly provided by Dr. Rudiger Rudolf, Karlsruhe, Germany.
- Entrez GeneID:
- 4644
- Protein Accession#:
- NP_000250.3;NP_001135967.1
- Gene Name:
- MYO5A
- Gene Alias:
- GS1,MYH12,MYO5,MYR12
- Gene Description:
- myosin VA (heavy chain 12, myoxin)
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq
- Other Designations:
- OTTHUMP00000174452,dilute,myosin V,myosin VA,myosin heavy chain 12,myosin, heavy polypeptide kinase,myoxin