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MEIG1 Rabbit pAb (bs-18778R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-18778R
英文名稱 MEIG1 Rabbit pAb
中文名稱 MEIG1蛋白抗體
別    名 bA2K17.3; meig1; MEIG1_HUMAN; Meiosis expressed gene 1 homolog; Meiosis expressed gene 1 protein homolog.  
研究領域 細胞生物  免疫學  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Dog,Horse)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,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 11 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 MEIG1: 31-80/88 
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 MEIG1 is an 88 amino acid protein that is thought to function in germ cell differentiation and belongs to the MEIG1 family. The gene encoding MEIG1 maps to human chromosome 10p13. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Function:
May be involved in germ cell differentiation.

Similarity:
Belongs to the MEIG1 family.

SWISS:
Q5JSS6

Gene ID:
644890

Database links:

Entrez Gene: 644890 Human

Omim: 614174 Human

SwissProt: Q5JSS6 Human

Unigene: 257249 Human



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