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Rabbit Anti-MMTAG2  antibody (bs-17690R)
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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-17690R
英文名称 MMTAG2
中文名称 多发性骨髓瘤相关蛋白2抗体
别    名 chromosome 1 open reading frame 35; C1orf35; hMMTAG2; MGC4174; Multiple myeloma tumor-associated protein 2.  
研究领域 肿瘤  细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 (predicted: Human,Mouse,Rat,Chicken,Pig,Cow,Rabbit,Sheep)
产品应用 ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 29kDa
细胞定位 细胞外基质 分泌型蛋白 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MMTAG2: 1-100/263 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C 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 MMTAG2 is a 263 amino acid protein that exists as four alternatively spliced isoforms that map to human chromosome 1q42.13. Chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Function:
MMTAG2 (multiple myeloma tumor-associated protein 2), also known as C1orf35 (chromosome 1 open reading frame 35), is a 263 amino acid protein that exists as four alternatively spliced isoforms that map to human chromosome 1q42.13. Chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

SWISS:
Q9BU76

Gene ID:
79169

Database links:

Entrez Gene: 79169 Human

SwissProt: Q9BU76 Human

SwissProt: Q99LX5 Mouse

SwissProt: Q5M9I6 Rat

Unigene: 445952 Human



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