FGF-2 Polyclonal Antibody
¥680.00
- 产品信息
商品描述
靶点-Target
WBSCR11
反应性
Human,Mouse,Rat
应用
WB,IHC,IF,ELISA
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Unmodified
MW(Observed)
106kD
推荐稀释比
WB 1:500-1:2000;IHC 1:100-1:300;ELISA 1:20000;IF 1:50-200
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
克隆性
Polyclonal
免疫原
The antiserum was produced against synthesized peptide derived from human GTF2IRD1. AA range:71-120
特异性
WBSCR11 Polyclonal Antibody detects endogenous levels of WBSCR11 protein.
基因名称
GTF2IRD1
蛋白名称
General transcription factor II-I repeat domain-containing protein 1
别名
GTF2IRD1;CREAM1;GTF3;MUSTRD1;RBAP2;WBSCR11;WBSCR12;General transcription factor II-I repeat domain-containing protein 1;GTF2I repeat domain-containing protein 1;General transcription factor III;MusTRD1/BEN;Muscle TFII-I repeat do
Organism-1
Human
基因ID-1
9569
SwissProt-1
Q9UHL9
Organism-2
Mouse
基因ID-2
57080
SwissProt-2
Q9JI57
背景
The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010],
细胞定位
Nucleus.
