深圳欣博盛生物科技有限公司 a1

Fibrillin 1 antibody [C3], C-term
货号:GTX101216 规格:100μl 目录价:¥4000
货号:GTX101216-S 规格:25μl 目录价:¥1700
产品详情
* 以下信息仅供参考,详情请以原厂网站为准
产品名称:
Fibrillin 1 antibody [C3], C-term
别名:
fibrillin 1 , ACMICD , ECTOL1 , FBN , GPHYSD2 , MASS , MFLS , MFS1 , OCTD , SGS , SSKS , WMS , WMS2
反应种属:
Human
宿主来源:
Rabbit
实验应用:
WB
同种型:
IgG
免疫原:
Recombinant protein encompassing a sequence within the C-terminus region of human Fibrillin 1. The exact sequence is proprietary.
克隆性:
Polyclonal
克隆号:
纯化方式:
Affinity purified by Protein A.
偶联:
Unconjugated
产品浓度:
2 mg/ml (Please refer to the vial label for the specific concentration.)
保存温度:
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
运输温度:
4°C
预期分子量:
312
产品形式:
Liquid
存储溶液:
PBS, 40% Glycerol, 0.01% Thimerosal.
生产商:
GeneTex
功能与背景:
This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome. [provided by RefSeq]
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