ELN polyclonal antibody
產(chǎn)品名稱： ELN polyclonal antibody
英文名稱： ELN polyclonal antibody
產(chǎn)品編號： PAB13513
產(chǎn)品價格： null
產(chǎn)品產(chǎn)地： 臺灣
品牌商標(biāo)： Abnova
更新時間： null
使用范圍：
亞諾法生技股份有限公司（Abnova)
- 聯(lián)系人 :
- 地址 : 臺灣臺北市內(nèi)湖區(qū)洲子街 108 號 9 樓
- 郵編 : 11493
- 所在區(qū)域 : 臺灣
- 電話 : +886-920**1152 點(diǎn)擊查看
- 傳真 : 點(diǎn)擊查看
- 郵箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Rabbit polyclonal antibody raised against native ELN.
- Immunogen:
- Native purified ELN from human skin.
- Host:
- Rabbit
- Reactivity:
- Human
- Specificity:
- This antibody reacts with human elastin, cross-reactivity in RIA at 1:500 dilution: human collagen type I, II, III, IV, V <0.1 %; human fibronectin <0.1%.
- Form:
- Lyophilized
- Storage Buffer:
- Lyophilized from purified antibody in PBS without addition BSA and preservative.
- Storage Instruction:
- Store at 4°C on dry atmosphere.
After reconstitution with 0.5 mL distilled water, store at -20°C or lower.
Aliquot to avoid repeated freezing and thawing.
- Recommend Usage:
- ELISA (>1:200)
Immunohistochemistry (1:500)
Immunofluorescence (1:80)
The optimal working dilution should be determined by the end user.
- Applications
- Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
- Immunohistochemical staining of paraffin-embedded human skin section. Using ELN polyclonal antibody (Cat # PAB13513) in combination with anti-rabbit IgG. HRPO and DAB, counter stained with Haemalaun. Note brown staining of ELN network of the dermis.
- Application Image
- Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
- enlarge
- Immunofluorescence
- ELISA
- Radioimmunoassay
- Entrez GeneID:
- 2006
- Gene Name:
- ELN
- Gene Alias:
- FLJ38671,FLJ43523,SVAS,WBS,WS
- Gene Description:
- elastin
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a protein that is one of the two components of elastic fibers. The encoded protein is rich in hydrophobic amino acids such as glycine and proline, which form mobile hydrophobic regions bounded by crosslinks between lysine residues. Deletions and mutations in this gene are associated with supravalvular aortic stenosis (SVAS) and autosomal dominant cutis laxa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
- Other Designations:
- OTTHUMP00000196667,tropoelastin
- Related Disease
- Alzheimer Disease
- Alzheimer disease
- Aneurysm, Ruptured
- Aortic Aneurysm, Abdominal
- Atherosclerosis
- Calcinosis
- Cardiovascular Diseases
- Chorioamnionitis
- Choroidal Neovascularization
- Coronary Artery Disease
- Diabetes Complications
- Diabetes Mellitus, Type 2
- Ductus Arteriosus, Patent
- Edema
- Emphysema
- Exfoliation Syndrome
- Fetal Membranes, Premature Rupture
- Genetic Predisposition to Disease
- Glaucoma