AB9279
视紫红质抗体
Chemicon®, from rabbit
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关于此项目
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
polyclonal
Application:
IHC
Species reactivity:
human
Citations:
8
Technique(s):
immunohistochemistry: suitable (paraffin)
Uniprot accession no.:
biological source
rabbit
conjugate
unconjugated
antibody form
affinity purified immunoglobulin
antibody product type
primary antibodies
clone
polyclonal
purified by
affinity chromatography
species reactivity
human
manufacturer/tradename
Chemicon®
technique(s)
immunohistochemistry: suitable (paraffin)
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Quality Level
Gene Information
human ... RHO(6010)
Application
在石蜡包埋的组织切片上的免疫组织化学分析。
最佳工作稀释度必须由最终用户进行确定。
最佳工作稀释度必须由最终用户进行确定。
研究子类别
感官 & PNS
感官 & PNS
研究类别
神经科学
神经科学
视紫红质抗体可检测视紫红质水平 & 已发表 & 经验证可用于IH(P)。
Biochem/physiol Actions
识别视紫红质。
Disclaimer
除非我们的产品目录或产品附带的其他公司文档另有说明，否则我们的产品仅供研究使用，不得用于任何其他目的，包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
Immunogen
来自人视紫红质第二胞外结构域的合成肽。
Other Notes
浓度：请参考批次特异性浓缩物的检验报告。
Physical form
亲和纯化的免疫球蛋白。 溶液，溶于含低于0.1%叠氮化钠的PBS中。
Preparation Note
接收后，以未稀释的等分试样在-70°C下保存长达6个月。应避免反复冻/融循环。
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Riccardo Natoli et al.
Molecular vision, 24, 201-217 (2018-03-13)
Systemic increases in reactive oxygen species, and their association with inflammation, have been proposed as an underlying mechanism linking obesity and age-related macular degeneration (AMD). Studies have found increased levels of oxidative stress biomarkers and inflammatory cytokines in obese individuals;
Riccardo Natoli et al.
Investigative ophthalmology & visual science, 58(7), 2977-2990 (2017-06-13)
Complement system dysregulation is strongly linked to the progression of age-related macular degeneration (AMD). Deposition of complement including C3 within the lesions in atrophic AMD is thought to contribute to lesion growth, although the contribution of local cellular sources remains
Kristin L Gardiner et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 28(1), 266-278 (2019-10-13)
The form of hereditary childhood blindness Leber congenital amaurosis (LCA) caused by biallelic RPE65 mutations is considered treatable with a gene therapy product approved in the US and Europe. The resulting vision improvement is well accepted, but long-term outcomes on
Isabel Pinilla et al.
Experimental eye research, 150, 122-134 (2015-11-03)
To characterize the relationship between fundus autofluorescence (FAF), Optical Coherence Tomography (OCT) and immunohistochemistry (IHC) over the course of chronic retinal degeneration in the P23H rat. Homozygous albino P23H rats, Sprague-Dawley (SD) rats as controls and pigmented Long Evans (LE)
Sizar Kamar et al.
International journal of molecular sciences, 21(2) (2020-01-18)
Biblical references aside, restoring vision to the blind has proven to be a major technical challenge. In recent years, considerable advances have been made towards this end, especially when retinal degeneration underlies the vision loss such as occurs with retinitis
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