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Merck
CN

AB748

抗IV型胶原抗体

Chemicon®, from rabbit

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
polyclonal
Species reactivity:
human
Application:
ELISA, IHC
Citations:
37
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biological source

rabbit

Quality Level

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable, immunohistochemistry: suitable

suitability

not suitable for immunohistochemistry (Paraffin), not suitable for Western blot

shipped in

dry ice

target post-translational modification

unmodified

Gene Information

human ... COL4A1(1282)

Immunogen

纯化人IV型胎盘胶原蛋白

Application

人IV型胶原蛋白ELISA:1:3,000

IV型胶原在人体组织低温切片上的间接免疫荧光可视化:1:20-1:40,仅限新鲜冷冻或丙酮固定标本。

斑点和狭缝印迹:1:300。

不推荐用于蛋白质印迹,也不推荐用于石蜡包埋组织切片。

最佳工作稀释度必须由最终用户进行确定。
抗IV型胶原抗体可检测IV型胶原水平,已发布,经验证可用于ELISA、RIA、IH、IH(P)。
研究子类别
ECM 蛋白
研究类别
细胞结构

Biochem/physiol Actions

抗体与天然和热变性人IV型胶原蛋白反应。 与I、III、V型胶原的交叉反应性小于10%,与人II型胶原的交叉反应性小于1%。 抗血清通过固定化的人血浆蛋白和人I、III、V型胶原蛋白。人血浆蛋白不干扰与胶原蛋白的结合。

Physical form

亲和纯化的交叉吸收抗血清抗体。 PBS溶液,含甘露醇、葡聚糖,不含防腐剂。
形式:纯化

Preparation Note

收到货后,在-20°C下以未稀释等分试样可保存长达12个月。应避免反复冻/融循环。

Other Notes

浓度:请参考批次特异性浓缩物的检验报告。

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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。


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存储类别

12 - Non Combustible Liquids

flash_point_f

Not applicable

flash_point_c

Not applicable



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Moa Lindgren et al.
Clinical & experimental metastasis, 38(2), 175-185 (2021-03-04)
No reliable, non-invasive biomarker of metastatic breast cancer (mBC) exists: circulating CA15-3 (cCA15-3) is the marker mostly used to monitor mBC. Circulating collagen IV (cCOLIV) has been evaluated in other metastatic cancers and has been found to be a promising
Yonghui Ding et al.
Advanced healthcare materials, 6(11) (2017-03-25)
Pathological modification of the subendothelial extracellular matrix (ECM) has closely been associated with endothelial activation and subsequent cardiovascular disease progression. To understand regulatory mechanisms of these matrix modifications, the majority of previous efforts have focused on the modulation of either
Distribution patterns of extracellular matrix components and adhesion receptors are intricately modulated during first trimester cytotrophoblast differentiation along the invasive pathway, in vivo.
Damsky, CH; Fitzgerald, ML; Fisher, SJ
The Journal of Clinical Investigation null



全球贸易项目编号

货号GTIN
AB74804053252325922