FANCA polyclonal antibody
产品名称: FANCA polyclonal antibody
英文名称: FANCA polyclonal antibody
产品编号: PAB10045
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:
- Rabbit polyclonal antibody raised against synthetic peptide of FANCA.
- Immunogen:
- A synthetic peptide corresponding to amino acids 995-1009 of human FANCA.
- Host:
- Rabbit
- Reactivity:
- Chimpanzee, Human
- Form:
- Liquid
- Storage Buffer:
- In 20 mM KH2PO4, 150 mM NaCl, pH 7.2 (0.01% sodium azide)
- Storage Instruction:
- Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Synthetic Peptide.
- Recommend Usage:
- ELISA (1:15000-1:60000)
Western Blot (1:500-1:3000)
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.
- Publication Reference
- 1.
- Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.
Smogorzewska A, Matsuoka S, Vinciguerra P, McDonald ER 3rd, Hurov KE, Luo J, Ballif BA, Gygi SP, Hofmann K, D'Andrea AD, Elledge SJ.Cell. 2007 Apr 20;129(2):289-301. Epub 2007 Apr 5.
- 2.
- A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer.
Thompson E, Dragovic RL, Stephenson SA, Eccles DM, Campbell IG, Dobrovic A.BMC Cancer. 2005 Apr 29;5:43.
- 3.
- Identification of multiple nuclear export sequences in Fanconi anemia group A protein that contribute to CRM1-dependent nuclear export.
Ferrer M, Rodriguez JA, Spierings EA, de Winter JP, Giaccone G, Kruyt FA.Hum Mol Genet. 2005 May 15;14(10):1271-81. Epub 2005 Mar 24.
- Applications
- Western Blot (Cell lysate)
- Western blot using FANCA polyclonal antibody (Cat # PAB10045) shows detection of a band at ~133 KDa (arrowhead) corres-ponding to FANCA in HeLa whole cell lysates.
The identity of the lower molecular weight bands is unknown, but may represent breakdown products.
Approximately 35 ug of lysate was separated by 4-20% Tris Glycine SDS-PAGE.
After blocking, the membrane was probed for 2 h at room temperature with the primary antibody diluted to 1:1,500.
The membrane was washed and reacted with a 1:10,000 dilution of IRDye™800 conjugated Gt-a-Rabbit IgG [H&L] for 45 min at room temperature (800 nm channel, green).
Molecular weight estimation was made by comparison to prestained MW markers indicated at left (700 nm channel, red).
IRDye™800 fluorescence images were captured using the Odyssey® Infrared Imaging System developed by LI-COR.
IRDye is a trademark of LI-COR, Inc.
- Western Blot (Transfected lysate)
- Western blot using FANCA polyclonal antibody (Cat # PAB10045) shows detection of FANCA only in FANCA transfected GM6914 cell lysates.
No staining is seen in lysates prepared from FANCA (-/-) cells in the absence of FANCA transfection.
Modified from Smogorzewska et al (2007) Cell 129, 289-301.
- Entrez GeneID:
- 2175
- Protein Accession#:
- NP_000126;O15360
- Gene Name:
- FANCA
- Gene Alias:
- FA,FA-H,FA1,FAA,FACA,FAH,FANCH,MGC75158
- Gene Description:
- Fanconi anemia, complementation group A
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq
- Other Designations:
- Fanconi anemia, complementation group H,Fanconi anemia, type 1
- Related Disease
- Adenocarcinoma
- Breast cancer
- Breast Neoplasms
- Cardiovascular Diseases
- Diabetes Mellitus, Type 2
- Disease Progression
- Edema
- Esophageal Neoplasms
- Fanconi Anemia
- Genetic Predisposition to Disease
- Kidney Failure, Chronic
- Lung Neoplasms
- Meningeal Neoplasms
- Meningioma
- Neoplasms, Glandular and Epithelial
- Ovarian cancer
- Ovarian Neoplasms
- Pancreatic Neoplasms
- Papillomavirus Infections