CHD7 polyclonal antibody
產品名稱： CHD7 polyclonal antibody
英文名稱： CHD7 polyclonal antibody
產品編號： PAB25712
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 peptide of CHD7.
- Immunogen:
- A synthetic peptide corresponding to 18 amino acids at N-terminus of human CHD7.
- Host:
- Rabbit
- Reactivity:
- Human, Mouse
- Specificity:
- Multiple isoforms of CHD7 are known to exist.
- Form:
- Liquid
- Purification:
- Peptide affinity purification
- Concentration:
- 1 mg/mL
- Isotype:
- IgG
- Storage Buffer:
- In PBS (0.02% sodium azide)
- Storage Instruction:
- Store at 4°C for three months. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- Western Blot (1-2 ug/mL)
Immunohistochemistry (5 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.
- Applications
- Western Blot (Cell lysate)
- Western blot analysis of CHD7 in SK-N-SH cell lysate with CHD7 polyclonal antibody (Cat # PAB25712) at (lane 1) 1 and (lane 2) 2 ug/mL.
- Entrez GeneID:
- 55636
- Protein Accession#:
- Q9P2D1
- Gene Name:
- CHD7
- Gene Alias:
- FLJ20357,FLJ20361,IS3,KAL5,KIAA1416
- Gene Description:
- chromodomain helicase DNA binding protein 7
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. [provided by RefSeq
- Other Designations:
- -
- Related Disease
- Abnormalities, Multiple
- Central Nervous System Diseases
- Choanal Atresia
- Cleft Lip
- Cleft Palate
- Coloboma
- Deafness
- Disease Models, Animal
- Ductus Arteriosus, Patent
- Facial Paralysis
- Genetic Diseases, Inborn
- Genetic Predisposition to Disease
- Heart Defects, Congenital
- Heart Diseases
- Infant, Premature, Diseases
- Kallmann Syndrome
- Mouth Diseases
- Spinal Diseases
- Syndrome