WNT1 monoclonal antibody, clone 10C8
产品名称： WNT1 monoclonal antibody, clone 10C8
英文名称： WNT1 monoclonal antibody, clone 10C8
产品编号： MAB10372
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 recombinant WNT1.
- Immunogen:
- Recombinant protein corresponding to human WNT1.
- Host:
- Mouse
- Theoretical MW (kDa):
- 41
- Reactivity:
- Human, Mouse
- Form:
- Liquid
- Storage Buffer:
- In ascites (0.03% sodium azide)
- Storage Instruction:
- Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- ELISA (1:10000)
Western Blot (1:500-1:2000)
Immunohistochemistry (1:200-1:1000)
Immunofluorescence (1:200-1:1000)
Flow cytometry (1:200-1:400)
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)
- Western blot analysis using WNT1 monoclonal antibody, clone 10C8 (Cat # MAB10372) against NIH/3T3 (1), 3T3L1 (2) and HeLa (3) cell lysate.
- Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
- Immunohistochemical analysis of paraffin-embedded human adrenal gland tissue using WNT1 monoclonal antibody, clone 10C8 (Cat # MAB10372) with DAB staining.
- Entrez GeneID:
- 7471
- Gene Name:
- WNT1
- Gene Alias:
- INT1
- Gene Description:
- wingless-type MMTV integration site family, member 1
- Omim ID:
- 164820
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region. [provided by RefSeq
- Other Designations:
- Wingless-type MMTV integration site family, member 1 (oncogene INT1)
- Related Disease