官网链接
折扣/货期| 货号：GTX127310 | 规格：100μl | 目录价：￥4000 |
| 货号：GTX127310-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:
Twist1/2 antibody
别名:
ACS3 antibody , B-HLH DNA binding protein antibody , BPES2 antibody , BPES3 antibody , CRS1 antibody , DERMO1 antibody , H-twist antibody , MGC117334 antibody , SCS antibody , TWIST antibody , TWIST homolog of drosophila antibody , TWIST1 antibody , TWIST2 antibody , bHLHa38 antibody , bHLHa39 antibody , class A basic helix-loop-helix protein 38 antibody , class A basic helix-loop-helix protein 39 antibody , dermis-expressed protein 1 antibody , twist homolog 2 (Drosophila) antibody , twist-related bHLH protein Dermo1 antibody , twist-related protein 1 antibody , twist-related protein 2 antibody
反应种属:
Drosophila, Human, Mouse, Rat
宿主来源:
Rabbit
实验应用:
IHC, IHC-P, WB
同种型:
IgG
免疫原:
Recombinant protein encompassing a sequence within the center region of human Twist1/2. The exact sequence is proprietary.
克隆性:
Polyclonal
克隆号:
纯化方式:
Purified by antigen-affinity chromatography.
偶联:
Unconjugated
产品浓度:
0.67 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
产品形式:
Liquid
存储溶液:
PBS, 20% Glycerol, 0.025% ProClin 300.
生产商:
GeneTex
功能与背景:
This gene encodes a basic helix-loop-helix (bHLH) transcription factor that plays an important role in embryonic development. The encoded protein forms both homodimers and heterodimers that bind to DNA E box sequences and regulate the transcription of genes involved in cranial suture closure during skull development. This protein may also regulate neural tube closure, limb development and brown fat metabolism. This gene is hypermethylated and overexpressed in multiple human cancers, and the encoded protein promotes tumor cell invasion and metastasis. Mutations in this gene cause Saethre-Chotzen syndrome in human patients, which is characterized by craniosynostosis, ptosis and hypertelorism. [provided by RefSeq, Aug 2017]
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