FANCG polyclonal antibody
產品名稱： FANCG polyclonal antibody
英文名稱： FANCG polyclonal antibody
產品編號： PAB6485
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:
- Goat polyclonal antibody raised against synthetic peptide of FANCG.
- Immunogen:
- A synthetic peptide corresponding to human FANCG.
- Sequence:
- LEEFRTSLPKSCDL
- Host:
- Goat
- Theoretical MW (kDa):
- 68.5
- Reactivity:
- Human
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Synthetic Peptide.
- Recommend Usage:
- ELISA (1:32000)
Western Blot (0.5-1 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 human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells.
Liu N, Lamerdin JE, Tucker JD, Zhou ZQ, Walter CA, Albala JS, Busch DB, Thompson LH.Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9232-7.
- Applications
- Western Blot (Cell lysate)
- FANCG polyclonal antibody (Cat # PAB6485) staining (0.5 ug/mL) of HeLa cell lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
- Entrez GeneID:
- 2189
- Protein Accession#:
- NP_004620.1
- 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