RAX2 MaxPab mouse polyclonal antibody (B01)
产品名称： RAX2 MaxPab mouse polyclonal antibody (B01)
英文名称： RAX2 MaxPab mouse polyclonal antibody (B01)
产品编号： H00084839-B01
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
- 传真 : +886-2-8751-1186
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Mouse polyclonal antibody raised against a full-length human RAX2 protein.
- Immunogen:
- RAX2 (NP_116142.1, 1 a.a. ~ 184 a.a) full-length human protein.
- Sequence:
- MFLSPGEGPATEGGGLGPGEEAPKKKHRRNRTTFTTYQLHQLERAFEASHYPDVYSREELAAKVHLPEVRVQVWFQNRRAKWRRQERLESGSGAVAAPRLPEAPALPFARPPAMSLPLEPWLGPGPPAVPGLPRLLGPGPGLQASFGPHAFAPTFADGFALEEASLRLLAKEHAQALDRAWPPA
- Host:
- Mouse
- Reactivity:
- Human
- Storage Buffer:
- No additive
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody reactive against mammalian transfected lysate.
- Note:
- For IHC and IF applications, antibody purification with Protein A will be needed prior to use.
- MSDS:
Download
- Applications
- Western Blot (Transfected lysate)
- Western Blot analysis of RAX2 expression in transfected 293T cell line (H00084839-T02) by RAX2 MaxPab polyclonal antibody.
Lane 1: RAX2 transfected lysate(20.10 KDa).
Lane 2: Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 84839
- GeneBank Accession#:
- NM_032753.2
- Protein Accession#:
- NP_116142.1
- Gene Name:
- RAX2
- Gene Alias:
- ARMD6,CORD11,MGC15631,QRX,RAXL1
- Gene Description:
- retina and anterior neural fold homeobox 2
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. [provided by RefSeq
- Other Designations:
- Q50-type retinal homeobox,retina and anterior neural fold homeobox like 1