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RabbitAnti-BRN4 Rabbit pAb  antibody (bs-20757R)
~~~促销,代码KXJ230206~~~
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-20757R
英文名称 BRN4 Rabbit pAb
中文名称 脑转录因子4蛋白抗体
别    名 BRAIN-4; BRN-4; BRN4; DFN3; DFNX2; OCT-9; OTF-9; OTF9; Slf; RHS2; PO3F4_HUMAN; POU3F4; Brain-specific homeobox/POU domain protein 4 (Brain-4 | Brn-4); Octamer-binding protein 9 (Oct-9); Octamer-binding transcription factor 9 (OTF-9); PO3F4_MOUSE; PO3F4_RA  
研究领域 肿瘤  细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
产品应用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 51 kDa
检测分子量 51
细胞定位 细胞核 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human BRN4: 1-100/361 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 Probable transcription factor which exert its primary action widely during early neural development and in a very limited set of neurons in the mature brain.Defects in POU3F4 are a cause of deafness X-linked type 2 (DFNX2) . A mixed type of deafness characterized by both conductive hearing loss resulting from stapes (perilymphatic gusher) fixation and progressive sensorineural deafness.

Function:
Probable transcription factor which exert its primary action widely during early neural development and in a very limited set of neurons in the mature brain.

Subunit:
Homodimer. Heterodimer with a RAR molecule. Binds DNA preferentially as a RAR/RXR heterodimer.

Subcellular Location:
Nucleus.

Tissue Specificity:
Brain specific.

DISEASE:
Defects in POU3F4 are a cause of deafness X-linked type 2 (DFNX2) [MIM:304400]. A mixed type of deafness characterized by both conductive hearing loss resulting from stapes (perilymphatic gusher) fixation and progressive sensorineural deafness.

Similarity:
Belongs to the POU transcription factor family. Class-3 subfamily.
Contains 1 homeobox DNA-binding domain.
Contains 1 POU-specific domain.

SWISS:
P49335

Gene ID:
5456

Database links:

Entrez Gene: 5456 Human

Entrez Gene: 18994 Mouse

Entrez Gene: 29589 Rat

Omim: 300039 Human

SwissProt: P49335 Human

SwissProt: P62515 Mouse

SwissProt: P62516 Rat

Unigene: 2229 Human

Unigene: 405149 Mouse

Unigene: 56946 Mouse

Unigene: 33030 Rat

 



产品图片
Sample: Brain (Mouse) Lysate at 40 ug Brain (Rat) Lysate at 40 ug Cerebellum (Mouse) Lysate at 40 ug Primary: Anti-BRN4 (bs-20757R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 51 kD Observed band size: 51 kD
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