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SOHLH2 Rabbit pAb (bs-12279R)  
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產品編號 bs-12279R
英文名稱 SOHLH2 Rabbit pAb
中文名稱 精子卵子結合生成堿性螺旋蛋白2抗體
別    名 FLJ20449; FLJ57222; Solh2; Spermatogenesis-and oogenesis-specific basic helix-loop-helix-containing protein 2; TEB1; SOLH2_HUMAN.  
Specific References  (1)     |     bs-12279R has been referenced in 1 publications.
[IF=3.45] Ding, Jin, et al. "Protection of Murine Spermatogenesis Against Ionizing Radiation-Induced Testicular Injury by a Green Tea Polyphenol." Biology of Reproduction (2014): biolreprod-114.  Mouse.  
研究領域 細胞生物  發育生物學  干細胞  轉錄調節因子  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat)
產品應用 ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 47 kDa
檢測分子量
細胞定位 細胞核 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from Human SOHLH2: 221-320/425 
亞    型 IgG
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 SOHLH2 is a 425 amino acid nuclear protein that contains one basic helix-loop-helix (bHLH) domain through which it may function as a transcription factor during oogenesis and spermatogenesis. SOHLH2 exists as two alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 13q13.3. Chromosome 13 houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4% of the human genome. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.

Function:
Sohlh2, spermatogenesis- and oogenesis-specific basic helix-loop-helix-containing protein 2, is a basic loop helix transcription factor. Sohlh2 is normally expressed in pre-meiotic germ cells and testis and involved in spermatogenesis and oogenesis. Male Sohlh2 deficient mice are infertile due to a block in spermatogenesis.

Subcellular Location:
Nuclear

Similarity:
Contains 1 bHLH (basic helix-loop-helix) domain.

SWISS:
Q9NX45

Gene ID:
54937

Database links:

Entrez Gene: 100526761 Human

Entrez Gene: 54937 Human

SwissProt: Q9NX45 Human

Unigene: 124519 Human



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