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Merck
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Key Documents

SAB4301605

Sigma-Aldrich

Anti-IL3RA

affinity isolated antibody

同義詞:

CD123, IL3R, IL3RAY, IL3RX, IL3RY

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

rabbit

品質等級

抗體表格

affinity isolated antibody

抗體產品種類

primary antibodies

無性繁殖

polyclonal

形狀

buffered aqueous glycerol solution

物種活性

human, mouse

技術

immunohistochemistry: 1:100-1:200
western blot: 1:500-1:2000

登錄號

NP_002174

UniProt登錄號

運輸包裝

wet ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... IL3RA(3563)

一般說明

Interleukin 3 receptor subunit α alpha (IL3RA or CD123) gene is localized in the X and Y chromosomes. It comprises a highly mobile N-terminal domain (NTD) region and fibronectin type III (FnIII) domain. CD123 is expressed on early hematopoietic cells and is a type I cytokine receptor.

免疫原

Synthetic peptide of human interleukin 3 receptor, alpha (low affinity)

生化/生理作用

Elevated expression of IL3RA is reported in chronic myeloid leukemia (CML).) It may serve as a therapeutic potential to treat acute myelogenous leukemia (AML).

特點和優勢

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

外觀

Rabbit IgG in pH7.4 PBS, 0.05% NaN3, 40% Glycerol.

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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C T Jordan et al.
Leukemia, 14(10), 1777-1784 (2000-10-06)
Recent studies suggest that the population of malignant cells found in human acute myelogenous leukemia (AML) arises from a rare population of leukemic stem cells (LSCs). LSCs have been documented for nearly all AML subtypes and have been phenotypically described
Prognostic relevance of CD123 expression in adult AML with normal karyotype.
Gina Jiang et al.
British journal of haematology, 188(1), 181-184 (2019-11-24)
M Joseph et al.
Journal of medical genetics, 33(11), 906-911 (1996-11-01)
Colony stimulating factor-2 receptor alpha (CSF2RA) and interleukin-3 receptor alpha (IL3RA), two genes from the chromosome Xp and Yp pseudoautosomal region (PAR), have been suggested as candidate genes for short stature in Turner syndrome. We report three girls with X;Y

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