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DLL3 Rabbit pAb (bs-7860R)  
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產品編號 bs-7860R
英文名稱 DLL3 Rabbit pAb
中文名稱 Notch信號通路Delta樣配體3抗體
別    名 delta Drosophila like 3; delta like 3 Drosophila; delta like 3 homolog Drosophila; delta like 3 protein; delta like protein 3 precursor; delta3; Drosophila delta homolog 3; SCDO1; Spondylocostal dysostosis autosomal recessive.DLL3_HUMAN  
Specific References  (1)     |     bs-7860R has been referenced in 1 publications.
[IF=2.886] Xiao Fu. et al. PD-L1 Predicts Poor Prognosis in Surgically Resected Limited Stage Small-Cell Lung Cancer. Cancer Manag Res. 2020; 12: 10939–10948  IHC ;  Human.  
研究領域 細胞生物  發育生物學  神經生物學  信號轉導  細胞周期蛋白  細胞分化  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Human,Mouse (predicted: Rabbit,Cow,Dog,Horse)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 65 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DLL3: 51-150/618 <Extracellular>
亞    型
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 Delta-like 3 (DLL3) is a transmembrane Delta-like protein that inhibits primary neurogenesis. It may be required to divert neurons along a specific differentiation pathway and plays a role in the formation of somite boundaries during segmentation of the paraxial mesoderm. DLL3 is one of five DSL proteins that bind to the Notch receptor and activates Notch signaling.

Function:
Inhibits primary neurogenesis. May be required to divert neurons along a specific differentiation pathway. Plays a role in the formation of somite boundaries during segmentation of the paraxial mesoderm.

Subunit:
Can bind and activate Notch-1 or another Notch receptor (Probable).

Subcellular Location:
Membrane; Single-pass type I membrane protein (Probable).

Tissue Specificity:
Predominantly expressed in the neuroectoderm and paraxial mesoderm during embryogenesis.

Post-translational modifications:
Ubiquitinated by MIB (MIB1 or MIB2), leading to its endocytosis and subsequent degradation.

DISEASE:
Note=A truncating mutation in Dll3 is the cause of the pudgy (pu) phenotype. Pudgy mice exhibit patterning defects at the earliest stages of somitogenesis. Adult pudgy mice present severe vertebral and rib deformities.

Similarity:
Contains 1 DSL domain.
Contains 6 EGF-like domains.

SWISS:
Q9NYJ7

Gene ID:
10683

Database links:

Entrez Gene: 505993 Cow

Entrez Gene: 10683 Human

Entrez Gene: 100520433 Pig

Omim: 602768 Human

SwissProt: Q9NYJ7 Human

Unigene: 127792 Human



產品圖片
Sample: Fetal brain (Mouse) Lysate at 40 ug Primary: Anti-DLL3 (bs-7860R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 65 kD Observed band size: 65 kD
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