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Merck
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FCMAB112F

Sigma-Aldrich

Anti-SOX-2 Antibody, clone 6G1.2, FITC conjugate

clone 6G1.2, from mouse, FITC conjugate

别名:

SRY (sex determining region Y)-box 2, SRY-related HMG-box gene 2, sex-determining region Y-box 2, transcription factor SOX2

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

mouse

品質等級

共軛

FITC conjugate

抗體表格

purified immunoglobulin

抗體產品種類

primary antibodies

無性繁殖

6G1.2, monoclonal

物種活性

human, rat, mouse

技術

flow cytometry: suitable

同型

IgG2b

NCBI登錄號

UniProt登錄號

運輸包裝

wet ice

目標翻譯後修改

unmodified

基因資訊

human ... SOX2(6657)
mouse ... Sox2(20674)
rat ... Sox2(499593)

一般說明

Sox-2 plays a key role in embryonic stem cell development, and has been shown to help stem cells maintain a pluripotent potential. It has also been shown to be associated with uncommitted dividing stem cell and precursor cells of the developing CNS.

特異性

SOX-2

應用

Anti-SOX-2 Antibody, clone 6G1.2, FITC conjugate is an antibody against SOX-2 for use in FC.

品質

Evaluated by flow cytometry on undifferentiated adult Rat hippocampal neural stem cells SCR022.
Optimal working dilutions must be determined by the end user.

標靶描述

~34 kDa

外觀

Purified mouse monoclonal IgG2b conjugated to FITC in PBS with less than 0.09% sodium azide and 15 mg/mL BSA.

分析報告

Control
Rat Neural Stem Cells.

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Breanna S Borys et al.
Biotechnology and bioengineering, 117(5), 1316-1328 (2020-01-22)
Embryonic stem cells (ESCs) have almost unlimited proliferation capacity in vitro and can retain the ability to contribute to all cell lineages, making them an ideal platform material for cell-based therapies. ESCs are traditionally cultured in static flasks on a
Thalia Jimenez et al.
American journal of cancer research, 10(10), 3487-3506 (2020-11-10)
Breast cancer remains a complex disease resulting in high mortality in women. A subset of cancer stem cell (CSC)-like cells expressing aldehyde dehydrogenase 1 (ALDH1) and SOX2/OCT4 are implicated in aggressive biology of specific subtypes of breast cancer. Targeting these

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