TITF1 MaxPab mouse polyclonal antibody (B01)
产品名称： TITF1 MaxPab mouse polyclonal antibody (B01)
英文名称： TITF1 MaxPab mouse polyclonal antibody (B01)
产品编号： H00007080-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 TITF1 protein.
- Immunogen:
- TITF1 (NP_003308.1, 1 a.a. ~ 371 a.a) full-length human protein.
- Sequence:
- MSMSPKHTTPFSVSDILSPLEESYKKVGMEGGGLGAPLAAYRQGQAAPPTAAMQQHAVGHHGAVTAAYHMTAAGVPQLSHSAVGGYCNGNLGNMSELPPYQDTMRNSASGPGWYGANPDPRFPAISRFMGPASGMNMSGMGGLGSLGDVSKNMAPLPSAPRRKRRVLFSQAQVYELERRFKQQKYLSAPEREHLASMIHLTPTQVKIWFQNHRYKMKRQAKDKAAQQQLQQDSGGGGGGGGTGCPQQQQAQQQSPRRVAVPVLVKDGKPCQAGAPAPGAASLQGHAQQQAQHQAQAAQAAAAAISVGSGGAGLGAHPGHQPGSAGQSPDLAHHAASPAALQGQVSSLSHLNSSGSDYGTMSCSTLLYGRTW
- 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 NKX2-1 expression in transfected 293T cell line (H00007080-T01) by NKX2-1 MaxPab polyclonal antibody.
Lane1:TITF1 transfected lysate(40.81 KDa).
Lane2:Non-transfected lysate. - Protocol Download
- Entrez GeneID:
- 7080
- GeneBank Accession#:
- NM_003317.3
- Protein Accession#:
- NP_003308.1
- Gene Name:
- NKX2-1
- Gene Alias:
- BCH,BHC,NK-2,NKX2.1,NKX2A,TEBP,TITF1,TTF-1,TTF1
- Gene Description:
- NK2 homeobox 1
- Gene Ontology:
- Hyperlink
- Other Designations:
- NK-2 homolog A,benign chorea,thyroid nuclear factor,thyroid transcription factor 1
- Related Disease
- Carcinoma, Papillary
- Cell Transformation, Neoplastic
- Colon cancer
- Congenital Hypothyroidism
- Foramen Ovale, Patent
- Genetic Predisposition to Disease
- Goiter, Nodular
- Hirschsprung Disease
- Obesity
- Ovarian Failure, Premature
- Polycystic Ovary Syndrome
- Puberty, Delayed
- Puberty, Precocious
- Stroke
- Thrombophilia
- Thyroid Neoplasms
- Tobacco Use Disorder