6-HEX Bioconjugation-Ready


Catalog Number: B2011373 (2.5 mg)
6-HEX Bioconjugation-Ready is a high quality amino-reactive fluorescent probe. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

Live enquiry about this product via Text/SMS: 1-858-900-3210.

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6-HEX Bioconjugation-Ready
Catalog number: B2011373
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 2.5 mg
Molecular Weight or Concentration: 680.1 g/mol
Supplied as: Lyophilized
Applications: molecular tool for various biochemical applications
Storage: -20 °C
Keywords: [6-carboxy-2′,4,4′,5′,7,7′-hexachlorofluorescein, SE
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

1: Chang LS, Duan HQ. (S,E)-N-Methyl-4-[(S)2,6,6-trimethyl-4-oxocyclo-hex-2-en-yl]but-3-en-2-aminium chloride Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 1;67(Pt 6):o1289.
2: Arvat E, Di Vito L, Lanfranco F, Broglio F, Giordano R, Benso A, Muccioli GP, Deghenghi R, Ghigo E. Tyr-Ala-Hexarelin, a synthetic octapeptide, possesses the same endocrine activities of Hexarelin and GHRP-2 in humans J Endocrinol Invest. 1999 Feb;22(2):91-7.
3: Hung WC, Ling XH, Chang CC, Hsu HF, Wang SW, Lee YC, Luo C, Lee YT, Houng JY. Inhibitory Effects of Siegesbeckia orientalis Extracts on Advanced Glycation End Product Formation and Key Enzymes Related to Metabolic Syndrome Molecules. 2017 Oct 21;22(10):1785.
4: Spinato S, Stacchi C, Lombardi T, Bernardello F, Messina M, Dovigo S, Zaffe D. Influence of abutment height and vertical mucosal thickness on early marginal bone loss around implants: A randomised clinical trial with an 18-month post-loading clinical and radiographic evaluation Int J Oral Implantol (Berl). 2020;13(3):279-290.
5: Slanina T, Ayub R, Toldo J, Sundell J, Rabten W, Nicaso M, Alabugin I, Fdez Galván I, Gupta AK, Lindh R, Orthaber A, Lewis RJ, Grönberg G, Bergman J, Ottosson H. Impact of Excited-State Antiaromaticity Relief in a Fundamental Benzene Photoreaction Leading to Substituted Bicyclo[3.1.0]hexenes J Am Chem Soc. 2020 Jun 24;142(25):10942-10954.
6: Mutafela RN, Mantero J, Jani Y, Thomas R, Holm E, Hogland W. Radiometrical and physico-chemical characterisation of contaminated glass waste from a glass dump in Sweden Chemosphere. 2020 Feb;241:124964.
7: Aimaretti G, Baffoni C, DiVito L, Bellone S, Grottoli S, Maccario M, Arvat E, Camanni F, Ghigo E. Comparisons among old and new provocative tests of GH secretion in 178 normal adults Eur J Endocrinol. 2000 Apr;142(4):347-52.
8: Meade CJ, Muacevic G, Ward P, Soyka R. Pulmonary pharmacology of DT-TX 30 SE, a potent selective combined thromboxane synthetase inhibitor and receptor antagonist, in guinea pigs Jpn J Pharmacol. 1996 Jun;71(2):119-27.
9: Arvat E, Maccagno B, Ramunni J, Giordano R, Broglio F, Gianotti L, Maccario M, Camanni F, Ghigo E. Interaction between glucagon and hexarelin, a peptidyl GH secretagogue, on somatotroph and corticotroph secretion in humans Eur J Endocrinol. 2000 Nov;143(5):601-6.
10: Arvat E, Ramunni J, Bellone J, Di Vito L, Baffoni C, Broglio F, Deghenghi R, Bartolotta E, Ghigo E. The GH, prolactin, ACTH and cortisol responses to Hexarelin, a synthetic hexapeptide, undergo different age-related variations Eur J Endocrinol. 1997 Dec;137(6):635-42.

Products Related to 6-HEX Bioconjugation-Ready can be found at Fluorescence

Additional information

Weight 48 oz
Dimensions 8 × 8 × 8 in

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