Abnova

TUFM Monoclonal Antibody (1A2)

Name: TUFM Monoclonal Antibody (1A2)
Brand: Abnova
SKU: H00007284-M03
Price: 6404.00 CNY
Availability: InStock

查看其他20个TUFM抗体

说明书

Certificates

实验方案

问题与答案

技术支持

说明书

Certificates

实验方案

问题与答案

技术支持

说明书

Certificates

实验方案

问题与答案

技术支持

Additional Information:

抗体检测数据 (1)

图: 1 / 1

TUFM Antibody (H00007284-M03) in WB

Western Blot analysis of TUFM expression in transfected 293T cell line by TUFM monoclonal antibody (M03), clone 1A2. Lane 1: TUFM transfected lysate(49.9 KDa). Lane 2: Non-transfected lysate. .

Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.

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产品信息

H00007284-M03

应用

建议稀释比

已发表文章

免疫印迹 (WB)

1-5 µg/mL

酶联免疫吸附实验 (ELISA)

10 µg/mL

免疫沉淀 (IP)

1-5 µg/mL

产品规格

种属反应

Human

宿主/亚型

Mouse / IgG1, kappa

分类

Monoclonal

类型

Antibody

克隆号

1A2

抗原

TUFM (AAH01633, 40 a.a. approximately 455 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

1 mg/mL

100 µg

纯化类型

Protein A

保存液

PBS, pH 7.4

内含物

no preservative

保存条件

-20°C, Avoid Freeze/Thaw Cycles

Ambient (domestic); Wet ice (international)

产品详细信息

Product may be used with Western Blot (Transfected lysate).

Immunogen sequence: PLLCRGLAVE AKKTYVRDKP HVNVGTIGHV DHGKTTLTAA TTKILAEGGG AKFKKYEEID NAPEERARGI TINAAHVEYS TAARHYAHTD CPGHADYVKN MITGTAPLDG CILVVAANDG PMPQTREHLL LARQIGVEHV VVYVNKADAV QDSEMVELVE LEIRELLTEF GYKGEETPVI VGSALCALEG RDPELGLKSV QKLLDAVDTY IPVPARDLEK PFLLPVEAVY SVPGRGTVVT GTLERGILKK GDECELLGHS KNIRTVVTGI EMFHKSLERA EAGDNLGALV RGLKREDLRR GLVMVKPGSI KPHQKVEAQV YILSKEEGGR HKPFVSHFMP VMFSLTWDMA CRIILPPEKE LAMPGEDLKF NLILRQPMIL EKGQRFTLRD GNRTIGTGLV TNTLAMTEEE KNIKWG

靶标信息

This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.

仅用于科研。不用于诊断过程。未经明确授权不得转售。