标签归档：ac

Lacto-N-biose I(Synonyms: Galβ1-3GlcNAc)

发表于由
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天然产物 糖类和糖苷 Saccharides and Glycosides

Lacto-N-biose I;(Synonyms: Galβ1-3GlcNAc)

Lacto-N-biose I (Galβ1-3GlcNAc) 来自幽门螺杆菌的 α1,2-focusyltransferase 酶受体，是一种内源性代谢产物。

Lacto-N-biose I(Synonyms: Galβ1-3GlcNAc)

Lacto-N-biose I Chemical Structure

CAS No. : 50787-09-2

规格 价格 是否有货
1 mg ￥4900 询问价格 货期
5 mg ￥11500 询问价格 货期

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生物活性

Lacto-N-biose I (Galβ1-3GlcNAc), as an endogenous metabolite, is an acceptor for the α1,2-fucosyltransferase enzyme from Helicobacter pylori[1].

体外研究
(In Vitro)

Lacto-N-biose I is an acceptor for the α1,2-fucosyltransferase enzyme from Helicobacter pylori[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

383.35

Formula

C14H25NO11
CAS 号

50787-09-2
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.
参考文献

  • [1]. Valli M, et al. Beta-1,3-galactosyltransferase and alpha-1,2-fucosyltransferase involved in the biosynthesis of type-1-chain carbohydrate antigens in human colon adenocarcinoma cell lines. Eur J Biochem. 1998;256(2):494-501.

Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA

发表于由

Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA;

Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA (compound 1) 是一种高亲和力的五肽，与 src SH2 域结合 (IC50≈1 µM)。Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA 是 src SH3-SH2：磷酸蛋白相互作用的抑制剂。

Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFAamp;;

Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA Chemical Structure

规格 是否有货
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250 mg ; 询价 ;
500 mg ; 询价 ;

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生物活性

Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA (compound 1) is a high-affinity pentapeptide to bind to the src SH2 domain (IC50≈1 µM). Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH TFA is an inhibitor for src SH3-SH2:phosphoprotein interactions[1].

分子量

917.73

Formula

C34H47F3N5O19P
Sequence Shortening

Ac–{Tyr(PO3H2)}-EEIE-OH
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]. G J Pacofsky, et al. Potent dipeptide inhibitors of the pp60c-src SH2 domain. J Med Chem. 1998 May 21;41(11):1894-908.

Ac-YVAD-CHO(Synonyms: L-709049)

发表于由

Ac-YVAD-CHO;(Synonyms: L-709049)

Ac-YVAD-CHO (L-709049) 是一种有效的、可逆的、特异性的四肽白介素 1β 转化酶 (ICE) 抑制剂，小鼠和人类 Ki 值分别为 3.0 和 0.76 nM。Ac-YVAD-CHO 可抑制成熟 IL-lβ 的产生。

Ac-YVAD-CHOamp;;(Synonyms: L-709049)

Ac-YVAD-CHO Chemical Structure

CAS No. : 143313-51-3

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

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生物活性

Ac-YVAD-CHO (L-709049) is a potent, reversible, specific tetrapeptide interleukin-lβ converting enzyme (ICE) inhibitor with mouse and human Ki values of 3.0 and 0.76 nM. Ac-YVAD-CHO can suppress the production of mature IL-lβ[1].

IC50 Target

IL-1β

3 nM (Ki)

IL-1β

0.76 nM (Ki)

体外研究
(In Vitro)

Ac-YVAD-CHO inhibits IL-1β in a dose-dependent manner, with mouse and human IC50 values of 2.5 and 0.7 μM. Ac-YVAD-CHO (0.01~100 μM) reduces the elevations of IL-lβ in the plasma and peritoneal fluid treated with LPS in a dose-related manner[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究
(In Vivo)

Ac-YVAD-CHO (10 mg/kg; i.p.; 1 hour) is absorbed from the peritoneal cavity, as well as cleared from the blood rapidly[1].
Ac-YVAD-CHO (50 mg/kg; i.p.; 1 hour) drops precipitously to approximately 1 and 0.2 μM at 30 and 60 minutes after injection[1].
Ac-YVAD-CHO (30 mg/kg; i.p.; 6 hours) suppresses IL-1β levels[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: CD1 female mice
Dosage: 10 mg/kg (Pharmacokinetic Analysis)
Administration: I.p.; 1 hour
Result: Absorbed from the peritoneal cavity, as well as cleared from the blood rapidly.
Animal Model: CD1 female mice
Dosage: 50 mg/kg (Pharmacokinetic Analysis)
Administration: I.p.; 1 hour
Result: Dropped precipitously to approximately 1 and 0.2 μM at 30 and 60 minutes after injection.
Animal Model: P. acnes-sensitized mice
Dosage: 30 mg/kg
Administration: I.p.; 6 hours
Result: Suppressed IL-1β levels.

分子量

492.52

Formula

C23H32N4O8
CAS 号

143313-51-3
Sequence Shortening

Ac-YVAD-CHO
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.
参考文献

  • [1]. Fletcher DS, et al. A synthetic inhibitor of interleukin-1 beta converting enzyme prevents endotoxin-induced interleukin-1 beta production in vitro and in vivo. J Interferon Cytokine Res. 1995;15(3):243-248.

Ac-RYYRWK-NH2 TFA

发表于由

Ac-RYYRWK-NH2 TFA;

Ac-RYYRWK-NH2 TFA 是一个有效的和选择性 nociceptin receptor (NOP) 部分激动剂。[3H]Ac-RYYRWK-NH2 TFA 结合鼠皮层膜的 ORL1 的Kd 为0.071 nM，但是对 µ-,κ- 或 δ 阿片受体没有亲和力。

Ac-RYYRWK-NH2 TFAamp;;

Ac-RYYRWK-NH2 TFA Chemical Structure

CAS No. : 408305-09-9

规格 是否有货
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250 mg ; 询价 ;
500 mg ; 询价 ;

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生物活性

Ac-RYYRWK-NH2 is a potent and selective partial agonist for the nociceptin receptor (NOP), [3H]Ac-RYYRWK-NH2 binds to rat cortical membranes ORL1 with a Kd of 0.071 nM, but has no affinity for µ-, κ- or δ-opioid receptors[1].

体外研究
(In Vitro)

[3H]ac-RYYRWK-NH2 binding to rat cortical membranes revealed a single high affinity site for [3H]ac-RYYRWK-NH2 (Kd=0.071 nM)[1].
Naloxone benzoylhydrazone displaced [3H]acRYYRWK-NH2 binding to rat cortical membranes (Ki=104 nM) and human ORL1 (Ki=136 nM) as well as [125I]Tyr14-NC-OH to ORL1 (Ki=37 nM) has no affinity for µ-, κ- or δ-opioid receptors[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

1126.19

Formula

C51H70F3N15O11
CAS 号

408305-09-9
Sequence Shortening

Ac-RYYRWK-NH2
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.
参考文献

  • [1]. C T Dooley, et al. Binding and in vitro activities of peptides with high affinity for the nociceptin/orphanin FQ receptor, ORL1.J Pharmacol Exp Ther. 1997 Nov;283(2):735-41.

    [2]. M Ho, et al, Characterization of the ORL(1) receptor on adrenergic nerves in the rat anococcygeus muscle. Br J Pharmacol. 2000 Sep;131(2):349-55.

Ac2-12

发表于由

Ac2-12;

Ac2-12 是一种膜联蛋白/脂皮质激素 1 (LC1) 模拟肽，可抑制嗜中性白细胞的外渗。Ac2-12 具有抗迁移作用，并在实验性炎症模型中抑制嗜中性白细胞的募集。

Ac2-12amp;;

Ac2-12 Chemical Structure

CAS No. : 256447-08-2

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

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生物活性

Ac2-12, an annexin/lipocortin 1 (LC1)-mimetic peptide, inhibit neutrophil extravasation. Ac2-12 has antimigratory action and inhibits recruitment of neutrophils in experimental inflammation models[1][2].

体内研究
(In Vivo)

Ac2-12 (i.v.; 6.7 mg/kg, ≈70 nmol per mouse), was found to mimic the actions of lipocortin 1 (LC1) and Ac2-26 in male Swiss Albino mice (10-15 g)[1].
Ac2-12 (100 μg) significantly reduces polymorphonuclear leukocyte (PMN) influx in wild-type C57BL/6 mice and is no longer active in FPR KO mice[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

1351.57

Formula

C63H94N14O17S
CAS 号

256447-08-2
Sequence Shortening

Ac-AMVSEFLKQAW
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]. L H Lim, et al. Promoting detachment of neutrophils adherent to murine postcapillary venules to control inflammation: effect of lipocortin 1. Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14535-9.

    [2]. M Perretti, et al. Involvement of the receptor for formylated peptides in the in vivo anti-migratory actions of annexin 1 and its mimetics. Am J Pathol. 2001 Jun;158(6):1969-73.

Ac-IEVDIDVE TFA

发表于由

Ac-IEVDIDVE TFA;

Ac-IEVDIDVE TFA 是一个短肽序列，末端是 Ac。

Ac-IEVDIDVE TFAamp;;

Ac-IEVDIDVE TFA Chemical Structure

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

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生物活性

Ac-IEVDIDVE TFA is a short peptide sequence with Ac at the end.

分子量

1087.06

Formula

C44H69F3N8O20
Sequence

Ac-Ile-Glu-Val-Asp-Ile-Asp-Val-Glu
Sequence Shortening

Ac-IEVDIDVE
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.

Ac-RYYRIK-NH2 TFA

发表于由

Ac-RYYRIK-NH2 TFA;

Ac-RYYRIK-NH2 TFA 是一种有效的 ORL1 部分激动剂，作为 ORL1 的内源性配体，在 CHO 细胞中 (Kd=1.5 nM)。Ac-RYYRIK-NH2 TFA 是 G 蛋白激活的特异性拮抗剂，竞争性拮抗 noc/OFQ 在大鼠脑膜和脑切面刺激 [35S]-GTPgS 结合 G 蛋白。

Ac-RYYRIK-NH2 TFAamp;;

Ac-RYYRIK-NH2 TFA Chemical Structure

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

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生物活性

Ac-RYYRIK-NH2 TFA is a potent and partial agonist on ORL1 transfected in CHO cells (Kd=1.5 nM) and behaves as a endogenous ligand of ORL1. Ac-RYYRIK-NH2 is a specific antagonist for the activation of G protein and competitively antagonizes the stimulation of [35S]-GTPgS binding to G proteins by nociceptin/orphanin FQ (noc/OFQ) in membranes and sections of rat brain[1].

IC50 Target

Kd: 1.5 nM (ORL1 in CHO cells)[1]
体内研究
(In Vivo)

Ac-RYYRIK-NH2 TFA (intracerebroventricularly (i.c.v.)) inhibits spontaneous locomotor activity in mice with an ID50 of 0.07 nmol. Co-administration of noc/OFQ and Ac-RYYRIK-NH2 lead to additive effects in Male Swiss mice[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

1053.13

Formula

C46H71F3N14O11
Sequence Shortening

Ac-RYYRIK-NH2
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.
参考文献

  • [1]. H Berger, et al. Antagonism by acetyl-RYYRIK-NH2 of G protein activation in rat brain preparations and of chronotropic effect on rat cardiomyocytes evoked by nociceptin/orphanin FQ. Br J Pharmacol. 1999 Feb;126(3):555-8.

    [2]. H Berger, et al. The nociceptin/orphanin FQ receptor ligand acetyl-RYYRIK-amide exhibits antagonistic and agonistic properties.Peptides. 2000 Jul;21(7):1131-9.

    [3]. C T Dooley, et al. Binding and in vitro activities of peptides with high affinity for the nociceptin/orphanin FQ receptor, ORL1. J Pharmacol Exp Ther. 1997 Nov;283(2):735-41.

AC 253

发表于由

AC 253;

AC 253 是 amylin 的拮抗剂，抑制 125I-adrenomedullin 结合，其IC50 值为 25 nM。

AC 253amp;;

AC 253 Chemical Structure

CAS No. : 151804-79-4

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

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生物活性

AC 253, an amylin antagonist, inhibits 125I-adrenomedullin binding, with an IC50 of 25 nM[1].

体外研究
(In Vitro)

AC 253 (5-20 μM) antagonizes adrenomedullin-stimulated cAMP production at micromolar concentrations[1].
AC 253 (5-10 μM) blocks increases in intracellular Ca2+, activation of protein kinase A, MAPK, Akt, cFos, and cell death, which occur upon AMY3 activation with hAmylin, Aβ1-42, or their co-application[2].
AC 253 (10 nM) blocks Aβ1-42-induced electrophysiological effects[3].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

2847.11

Formula

C122H196N40O39
CAS 号

151804-79-4
Sequence

Ac-Leu-Gly-Arg-Leu-Ser-Gln-Glu-Leu-His-Arg-Leu-Gln-Thr-Tyr-Pro-Arg-Thr-Asn-Thr-Gly-Ser-Asn-Thr-Tyr-NH2
Sequence Shortening

Ac-LGRLSQELHRLQTYPRTNTGSNTY-NH2
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.
参考文献

  • [1]. H A Coppock, et al. Rat-2 fibroblasts express specific adrenomedullin receptors, but not calcitonin-gene-related-peptide receptors, which mediate increased intracellular cAMP and inhibit mitogen-activated protein kinase activity. Biochem J. 1999 Feb 15;338 ( Pt 1)(Pt 1):15-22.

    [2]. Wen Fu, ET AL. Amyloid β (Aβ) peptide directly activates amylin-3 receptor subtype by triggering multiple intracellular signaling pathways. J Biol Chem. 2012 May 25;287(22):18820-30.

    [3]. Jack H Jhamandas, et al. Actions of β-amyloid protein on human neurons are expressed through the amylin receptor. Am J Pathol. 2011 Jan;178(1):140-9.

Ac2-12 TFA

发表于由

Ac2-12 TFA;

Ac2-12 TFA 是一种膜联蛋白/脂皮质激素 1 (LC1) 模拟肽，可抑制嗜中性白细胞的外渗。Ac2-12 TFA 具有抗迁移作用，并在实验性炎症模型中抑制嗜中性白细胞的募集。

Ac2-12 TFAamp;;

Ac2-12 TFA Chemical Structure

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

* Please select Quantity before adding items.

生物活性

Ac2-12 TFA, an annexin/lipocortin 1 (LC1)-mimetic peptide, inhibit neutrophil extravasation. Ac2-12 TFA has antimigratory action and inhibits recruitment of neutrophils in experimental inflammation models[1][2].

体内研究
(In Vivo)

Ac2-12 TFA (i.v.; 6.7 mg/kg, ≈70 nmol per mouse), was found to mimic the actions of lipocortin 1 (LC1) and Ac2-26 in male Swiss Albino mice (10-15 g)[1].
Ac2-12 TFA (100 μg) significantly reduces polymorphonuclear leukocyte (PMN) influx in wild-type C57BL/6 mice and is no longer active in FPR KO mice[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

1465.59

Formula

C65H95F3N14O19S
Sequence Shortening

Ac-AMVSEFLKQAW
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]. L H Lim, et al. Promoting detachment of neutrophils adherent to murine postcapillary venules to control inflammation: effect of lipocortin 1. Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14535-9.

    [2]. M Perretti, et al. Involvement of the receptor for formylated peptides in the in vivo anti-migratory actions of annexin 1 and its mimetics. Am J Pathol. 2001 Jun;158(6):1969-73.

Dentonin(Synonyms: AC-100)

发表于由

Dentonin;(Synonyms: AC-100)

Dentonin (AC-100) 是 MEPE 来源的短肽片段。Dentonin 通过促进骨祖细胞粘附而促进成骨作用，并且可以促进未成熟的贴壁细胞存活。Dentonin 对成熟成骨细胞无显著影响。Dentonin 可用于磷酸盐稳态和骨代谢的研究。

Dentoninamp;;(Synonyms: AC-100)

Dentonin Chemical Structure

CAS No. : 400090-20-2

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

* Please select Quantity before adding items.

生物活性

Dentonin (AC-100) is a synthetic fragment derived from MEPE. Dentonin enhances osteogenesis by promoting osteoprogenitor adhesion and facilitates immature adherent cells survival. Dentonin has no significant effect to mature osteoblasts. Dentonin can be used for the research of phosphate homeostasis and bone metabolism[1].

体外研究
(In Vitro)

MEPE is a a member of the SIBLING (Small Integrin-Binding Ligand, N-linked Glycoprotein) family of secreted glycophosphoproteins.  MEPE  regulates bone mass and influence osteoblast activity.[1].
Dentonin (3-30 μg/ml; 2-24 hours) significantly increases the numbers of cell and shows enhanced promotion of cell adhesion. However, it has no significant differences in terms of numbers of cells adhered[2].
Dentonin (3-30 μg/ml; 2-24 hours) enhances osteoblast spreading, it exhibits significantly increased cell areas compared to all other treatment[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

2538.59

Formula

C107H160N30O42
CAS 号

400090-20-2
Sequence Shortening

TDLQERGDNDISPFSGDGQPFKD
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.
参考文献

  • [1]. Andrew P Sprowson, et al. ASARM-truncated MEPE and AC-100 enhance osteogenesis by promoting osteoprogenitor adhesion. J Orthop Res. 2008 Sep;26(9):1256-62.

    [2]. N Six, et al. Dentonin, a MEPE fragment, initiates pulp-healing response to injury.J Dent Res. 2007 Aug;86(8):780-5.