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Merck

O1136

Sigma-Aldrich

Monoclonal Anti-Ornithine Decarboxylase (ODC) antibody produced in mouse

clone ODC-29, ascites fluid

别名:

Ornithine Decarboxylase Antibody, Ornithine Decarboxylase Antibody - Monoclonal Anti-Ornithine Decarboxylase (ODC) antibody produced in mouse

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About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

mouse

共軛

unconjugated

抗體表格

ascites fluid

抗體產品種類

primary antibodies

無性繁殖

ODC-29, monoclonal

分子量

antigen 53 kDa

包含

15 mM sodium azide

物種活性

human, mouse

技術

immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
immunoprecipitation (IP): suitable
indirect ELISA: suitable
microarray: suitable
western blot: 1:100

同型

IgG2b

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... ODC1(4953)
mouse ... Odc1(18263)

一般說明

Monoclonal Anti-Ornithine Decarboxylase (ODC) (mouse IgG2b isotype) is derived from the ODC-29 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from immunized BALB/c mice. Its amino acid sequence is well conserved among species; the overall identity of the amino acid sequences of mouse, rat and human ODC proteins is greater than 90%.
Ornithine decarboxylase (ODC) levels increase rapidly after implantation during mouse embryogenesis. The gene encoding this protein is localized on mouse chromosome 12 and human chromosome 2.

特異性

By immunohistochemical staining of formalin-fixed, paraffin-embedded human prostate and colon carcinoma, the labeling is confined to epithelial cells.

免疫原

recombinant mouse ornithine decarboxylase.

應用

Monoclonal Anti-Ornithine Decarboxylase (ODC) antibody produced in mouse has been used in Western blotting.
Monoclonal Anti-Ornithine Decarboxylase (ODC) has also been used in enzyme linked immunosorbent assay (ELISA), immunoprecipitation, immunoblotting and immunohistochemistry.

生化/生理作用

Ornithine Decarboxylase (ODC) biological activity is rapidly induced to promote cell proliferation in response to hormones, drugs, growth factors, mitogens and tumour promoters. ODC mRNA levels are also elevated in transformed cells including lung carcinomas and human colon adenomas and carcinomas. ODC activity in colorectal carcinomas has been shown to be greater than that in adenomas, which, in turn, is greater than that of normal mucosa. ODC has a half-life of 8-30 min, the shortest half-life time reported in eukaryotic cells.
Ornithine decarboxylase (ODC) converts L-ornithine to putrescine. It has a role in cell replication. ODC is also involved in the polyamine synthesis pathway. The protein is upregulated in cancers. Overexpression of ODC has been associated with carcinogenesis in mice.

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Myc confers androgen-independent prostate cancer cell growth
David Bernard
The Journal of Clinical Investigation, 112(11), 1724?1731-1724?1731 (2003)
Su Xiao et al.
Biotechnology and bioengineering, 113(11), 2403-2415 (2016-05-25)
For the purpose of improving recombinant protein production from mammalian cells, an unbiased, high-throughput whole-genome RNA interference screen was conducted using human embryonic kidney 293 (HEK 293) cells expressing firefly luciferase. A 21,585 human genes were individually silenced with three
The methyl-CpG-binding protein MECP2 is required for prostate cancer cell growth
David Bernard
Oncogene, 25, 1358?1366-1358?1366 (2006)
Ornithine Decarboxylase (ODC) Expression Pattern in Human Prostate Tissues and ODC Transgenic Mice
Lei Young
The Journal of Histochemistry and Cytochemistry, 54(2) (2006)
Tissue microarray analysis of eIF4E and its downstream effector proteins in human breast cancer
Kleiner HE, et al.
Journal of Experimental & Clinical Cancer Research, 28(1), 5-5 (2009)

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