biological source
microbial
form
powder
mol wt
0.6-1.1 MDa
storage temp.
−20°C
InChI
1S/C28H44N2O23.Na/c1-5(33)29-9-18(11(35)7(3-31)47-25(9)46)49-28-17(41)15(39)20(22(53-28)24(44)45)51-26-10(30-6(2)34)19(12(36)8(4-32)48-26)50-27-16(40)13(37)14(38)21(52-27)23(42)43;/h7-22,25-28,31-32,35-41,46H,3-4H2,1-2H3,(H,29,33)(H,30,34)(H,42,43)(H,44,45);/q;+1/t7-,8-,9-,10-,11-,12-,13+,14+,15-,16-,17-,18-,19-,20+,21+,22+,25-,26+,27-,28-;/m1./s1
InChI key
YWIVKILSMZOHHF-QJZPQSOGSA-N
Application
HA is used in many applications including, cell culture, tissue engineering, and the study of wound healing.
Biochem/physiol Actions
Hyaluronic acid (HA) is an anionic linerar glycosaminoglycan composed of monomers of glurcuronic acid and N-acetylglucosamine. HA is widely distributed throughout connective and epithelial tissue and is a chief component of the extracellular matrix. HA contributes to cellular proliferation and may contribute to the progression of malignant tumors.
Features and Benefits
This Hyaluronic acid is animal-component free and produced using a proprietary process that uses minimal media and a water-based technology that eliminates the need for organic solvents.
Legal Information
A product of Novozyme Corp.
保管分類
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
H5542-10MG: + H5542-BULK: + H5542-VAR: + H5542-50MG:
jan