Tos-Gly-Pro-Arg-ANBA-IPA acetate Chemical Structure
CAS No. : 2070009-46-8
规格
价格
是否有货
数量
10;mM;*;1 mL in Water
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In-stock
5 mg
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In-stock
10 mg
¥5000
In-stock
50 mg
¥15000
In-stock
100 mg
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询价
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200 mg
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询价
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Tos-Gly-Pro-Arg-ANBA-IPA acetate 相关产品
bull;相关化合物库:
Bioactive Compound Library Plus
Peptide Library
生物活性
Tos-Gly-Pro-Arg-ANBA-IPA (tos-GPR-ANBA-IPA) acetate is a chromogenic peptide substrate. Tos-Gly-Pro-Arg-ANBA-IPA acetate can be used for luminescence measurement[1].
分子量
747.82
Formula
C32H45N9O10S
CAS 号
2070009-46-8
Sequence
Tos-Gly-Pro-Arg-ANBA-IPA
Sequence Shortening
Tos-GPR-ANBA-IPA
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Hafner G, et al. Evaluation of an automated chromogenic substrate assay for the rapid determination of hirudin in plasma. Thromb Res. 1995;77(2):165-173.
Tos-Gly-Pro-Arg-ANBA-IPA is a chromogenic peptide substrate. Tos-Gly-Pro-Arg-ANBA-IPA can be used for luminescence measurement[1].
分子量
687.77
Formula
C30H41N9O8S
CAS 号
99700-50-2
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
Solvent Solubility
In Vitro:;
H2O
Peptide Solubility and Storage Guidelines:
1.;;Calculate the length of the peptide.
2.;;Calculate the overall charge of the entire peptide according to the following table:
;
Contents
Assign value
Acidic amino acid
Asp (D), Glu (E), and the C-terminal -COOH.
-1
Basic amino acid
Arg (R), Lys (K), His (H), and the N-terminal -NH2
+1
Neutral amino acid
Gly (G), Ala (A), Leu (L), Ile (I), Val (V), Cys (C), Met (M), Thr (T), Ser (S), Phe (F), Tyr (Y), Trp (W), Pro (P), Asn (N), Gln (Q)
0
3.;;Recommended solution:
Overall charge of peptide
Details
Negative (lt;0)
1.;;Try to dissolve the peptide in water first. 2.;;If water fails, add NH4OH (lt;50 μL). 3.;;If the peptide still does not dissolve, add DMSO (50-100 μL) to solubilize the peptide.
Positive (gt;0)
1.;;Try to dissolve the peptide in water first. 2.;;If water fails, try dissolving the peptide in a 10%-30% acetic acid solution. 3.;;If the peptide still does not dissolve, try dissolving the peptide in a small amount of DMSO.
Zero (=0)
1.;;Try to dissolve the peptide in organic solvent (acetonitrile, methanol, etc.) first. 2.;;For very hydrophobic peptides, try dissolving the peptide in a small amount of DMSO, and then dilute the solution with water to the desired concentration.
参考文献
[1]. Hafner G, et al. Evaluation of an automated chromogenic substrate assay for the rapid determination of hirudin in plasma. Thromb Res. 1995;77(2):165-173.