Click-IT™ Tetramethylrhodamine (TAMRA) Protein Analysis Detection Kit
Click-IT™ Tetramethylrhodamine (TAMRA) Protein Analysis Detection Kit
Invitrogen™

Click-IT™ Tetramethylrhodamine (TAMRA) Protein Analysis Detection Kit

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The Click-iT™ Tetramethylrhodamine (TAMRA) Glycoprotein Detection Kit provides the second part of the simple and robust two-step technique to identify자세히 알아보기
Have Questions?
카탈로그 번호수량
C333701 Kit
카탈로그 번호 C33370
제품 가격(KRW)
645,000
온라인 행사
Ends: 31-Mar-2026
758,000
할인액 113,000 (15%)
Each
카트에 추가하기
수량:
1 Kit
제품 가격(KRW)
645,000
온라인 행사
Ends: 31-Mar-2026
758,000
할인액 113,000 (15%)
Each
카트에 추가하기
The Click-iT™ Tetramethylrhodamine (TAMRA) Glycoprotein Detection Kit provides the second part of the simple and robust two-step technique to identify and characterize glycoproteins by one- or two-dimensional gel electrophoresis. In step two, after the incorporation of the azide handle into protein glycan structures with either a Click-iT™ metabolic labeling reagent or the Click-iT™ Enzymatic Labeling system, the azide-modified glycoproteins are detected via the chemoselective ligation or click reaction between an azide and an alkyne. Gels with TAMRA labeled glycoproteins can be subsequently stained with the Multiplexed Proteomics™ technologies, SYPRO™ Ruby total protein stain and PRO-Q™ Emerald glycoprotein stain for the differential analysis of glycoprotein subclasses, total proteins and total glycoproteins in the same gel. Click-iT™ modified glycoproteins are also compatible with downstream LC-MS/MS and MALDI MS analysis for identification.
For Research Use Only. Not for use in diagnostic procedures.
사양
검출 방법Fluorescence
그린 기능Less hazardous
라벨링 타겟Proteins (Glycoproteins)
라벨 또는 염료TAMRA™ Isomers, TMR (Tetramethylrhodamine)
제품 유형TAMRA Protein Analysis Detection Kit
수량1 Kit
배송 조건Room Temperature
제품라인Click-iT
Unit SizeEach
구성 및 보관
Store in freezer -5°C to -30°C.

자주 묻는 질문(FAQ)

I am using Click-iT AHA (L-azidohomoalanine) kit to label nascent proteins in live cells, then detecting with TAMRA alkyne after fixation and permeabilization and a click reaction. But I'm seeing nucleolar labeling in the cells. It this expected?

Yes. All proteins synthesized during the time the AHA is present will be detected, and they may be all over the cell. Our imaging shows strong labeling in the nucleoli and cytoplasm, as well as nuclear labeling.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

인용 및 참조 문헌 (5)

인용 및 참조 문헌
Abstract
Protein synthesis in distal axons is not required for growth cone responses to guidance cues.
Authors:Roche FK, Marsick BM, Letourneau PC,
Journal:J Neurosci
PubMed ID:19158291
'Recent evidence suggests that growth cone responses to guidance cues require local protein synthesis. Using chick neurons, we investigated whether protein synthesis is required for growth cones of several types to respond to guidance cues. First, we found that global inhibition of protein synthesis stops axonal elongation after 2 h. ... More
Direct in-gel fluorescence detection and cellular imaging of O-GlcNAc-modified proteins.
Authors:Clark PM, Dweck JF, Mason DE, Hart CR, Buck SB, Peters EC, Agnew BJ, Hsieh-Wilson LC,
Journal:J Am Chem Soc
PubMed ID:18683930
'We report an advanced chemoenzymatic labeling strategy for direct fluorescence detection of O-GlcNAc proteins in gels that facilitates proteomic studies and greatly extend the reach of existing technologies. These new tools also enable the expression and dynamics of O-GlcNAc modifications to be monitored by imaging in cells and tissues. ... More
The cytoplasmic tail dileucine motif LL572 determines the glycosylation pattern of membrane-type 1 matrix metalloproteinase.
Authors:Ludwig T, Theissen SM, Morton MJ, Caplan MJ,
Journal:J Biol Chem
PubMed ID:18955496
'Membrane-type 1 matrix metalloproteinase (MT1-MMP; MMP-14) drives fundamental physiological and pathological processes, due to its ability to process a broad spectrum of substrates. Because subtle changes in its activity can produce profound physiological effects, MT1-MMP is tightly regulated. Currently, many aspects of this regulation remain to be elucidated. It has ... More
A novel approach to tag and identify geranylgeranylated proteins.
Authors:Chan LN, Hart C, Guo L, Nyberg T, Davies BS, Fong LG, Young SG, Agnew BJ, Tamanoi F,
Journal:Electrophoresis
PubMed ID:19784953
A recently developed proteomic strategy, the
Regulation of calcium/calmodulin-dependent kinase IV by O-GlcNAc modification.
Authors:Dias WB, Cheung WD, Wang Z, Hart GW,
Journal:J Biol Chem
PubMed ID:19506079
Similar to phosphorylation, GlcNAcylation (the addition of O-GlcNAc to Ser(Thr) residues on polypeptides) is an abundant, dynamic, and inducible post-translational modification. GlcNAcylated proteins are crucial in regulating virtually all cellular processes, including signaling, cell cycle, and transcription. Here we show that calcium/calmodulin-dependent kinase IV (CaMKIV) is highly GlcNAcylated in vivo. ... More