FANCG (phospho S383) polyclonal antibody
產品名稱: FANCG (phospho S383) polyclonal antibody
英文名稱: FANCG (phospho S383) polyclonal antibody
產品編號: PAB15907
產品價格: null
產品產地: 臺灣
品牌商標: Abnova
更新時間: null
使用范圍:
亞諾法生技股份有限公司(Abnova)
- 聯系人 :
- 地址 : 臺灣臺北市內湖區洲子街 108 號 9 樓
- 郵編 : 11493
- 所在區域 : 臺灣
- 電話 : +886-920**1152 點擊查看
- 傳真 : 點擊查看
- 郵箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Rabbit polyclonal antibody raised against synthetic phosphopeptide of FANCG.
- Immunogen:
- Synthetic phosphopeptide corresponding to residues surrounding S383 of human FANCG.
- Host:
- Rabbit
- Reactivity:
- Human
- Form:
- Liquid
- Storage Buffer:
- In PBS, pH 7.2 (50% glycerol, 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.
- Recommend Usage:
- ELISA (1:2000-1:5000)
Western Blot (1 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.
- Publication Reference
- 1.
- The consensus coding sequences of human breast and colorectal cancers.
Sjoblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, Mandelker D, Leary RJ, Ptak J, Silliman N, Szabo S, Buckhaults P, Farrell C, Meeh P, Markowitz SD, Willis J, Dawson D, Willson JK, Gazdar AF, Hartigan J, Wu L, Liu C, Parmigiani G, Park BH, Bachman KE, Papadopoulos N, Vogelstein B, Kinzler KW, Velculescu VE.Science. 2006 Oct 13;314(5797):268-74. Epub 2006 Sep 7.
- 2.
- X-linked inheritance of Fanconi anemia complementation group B.
Meetei AR, Levitus M, Xue Y, Medhurst AL, Zwaan M, Ling C, Rooimans MA, Bier P, Hoatlin M, Pals G, de Winter JP, Wang W, Joenje H.Nat Genet. 2004 Nov;36(11):1219-24. Epub 2004 Oct 24.
- 3.
- Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
Demuth I, Wlodarski M, Tipping AJ, Morgan NV, de Winter JP, Thiel M, Grasl S, Schindler D, D'Andrea AD, Altay C, Kayserili H, Zatterale A, Kunze J, Ebell W, Mathew CG, Joenje H, Sperling K, Digweed M.Eur J Hum Genet. 2000 Nov;8(11):861-8.
- Application Image
- Western Blot
- ELISA
- Entrez GeneID:
- 2189
- Gene Name:
- FANCG
- Gene Alias:
- FAG,XRCC9
- Gene Description:
- Fanconi anemia, complementation group G
- Omim ID:
- 602956
- 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 G. [provided by RefSeq
- Other Designations:
- DNA repair protein XRCC9,OTTHUMP00000021319,X-ray repair complementing defective repair in Chinese hamster cells 9,X-ray repair, complementing defective, in Chinese hamster, 9
- Related Disease
- Adenocarcinoma
- Ataxia telangiectasia
- Breast cancer
- Breast Neoplasms
- Carcinoma, Non-Small-Cell Lung
- Cardiovascular Diseases
- Colorectal Neoplasms
- Diabetes Mellitus, Type 2
- DNA Damage
- Edema
- Esophageal Neoplasms
- Genetic Predisposition to Disease
- Head and Neck Neoplasms
- Laryngeal Neoplasms
- Lung Neoplasms
- Mouth Neoplasms
- Neoplasms, Glandular and Epithelial
- Ovarian cancer
- Ovarian Neoplasms
