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SCP0161

[D-Ala²]-Growth Hormone Releasing Factor 1-29 amide human

Name: [D-Ala<SUP>2</SUP>]-Growth Hormone Releasing Factor 1-29 amide human
Brand: SIGMA

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About This Item

经验公式（希尔记法）:

C₁₄₉H₂₄₆N₄₄O₄₂S₁

分子量:

3357.88

UNSPSC代码:

12352209

NACRES:

NA.32

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Sigma-Aldrich

G6771

Growth Hormone Releasing Factor Fragment 1-29 amide human

Sigma-Aldrich

G9416

Glucagon-Like Peptide 1 Fragment 7-37 human

Sigma-Aldrich

G3265

Glucagon-Like Peptide I human

Sigma-Aldrich

T3410

Thymosin α₁ bovine

Roche

RNASEA-RO

RNase A

Sigma-Aldrich

SCP0153

GLP-1 (Preproglucagon 72-107 amide) (GLP-1 human)

Sigma-Aldrich

SML1719

BPC 157 trifluoroacetate salt

Sigma-Aldrich

G4535

[D-Lys³]-GHRP-6

Sigma-Aldrich

E7144

毒晰外泌肽-4

Sigma-Aldrich

I2643

胰岛素人

方案

≥95% (HPLC)

表单

lyophilized

组成

Peptide Content, ≥72%

储存条件

protect from light

储存温度

−20°C

Amino Acid Sequence

Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2

应用

Growth Hormone Releasing Factor (GHRF) is an amino acid peptide that induces the release of growth hormone via GPCR receptor GHRH-R. N-terminal fragments and modified fragments are used to study the biological roles of GHRF.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

监管及禁止进口产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

LI0776

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Enhanced stability and potency of novel growth hormone-releasing factor (GRF) analogues derived from rodent and human GRF sequences.

Campbell RM, Stricker P, Miller R, et al.

Peptide, 15, 489-495 (1994)

Position 2 and position 2/Ala15-substituted analogs of bovine growth hormone-releasing factor (bGRF) with enhanced metabolic stability and improved in vivo bioactivity.

T M Kubiak et al.

Journal of medicinal chemistry, 36(7), 888-897 (1993-04-02)

In order to prepare GRF analogs with high activity in vivo, a strategy was undertaken to stabilize the peptide to dipeptidylpeptidase IV (DPP-IV), a protease found in plasma which inactivates native human and bovine GRF by cleavage of the Ala2-Asp3

Pegylated peptides. IV. Enhanced biological activity of site-directed pegylated GRF analogs.

A M Felix et al.

International journal of peptide and protein research, 46(3-4), 253-264 (1995-09-01)

Conditions have been developed for the site-specific pegylation (NH2-terminus, side-chain and carboxy-terminus) of a potent analog of growth hormone-releasing factor, [Ala15]-hGRF(1-29)-NH2. These pegylated peptides were prepared by solid-phase peptide synthesis using the Fmoc/tBu strategy, and were fully characterized by analytical

Plasma growth hormone (GH) response to intravenous GH-releasing factor (GRF) in adult rats: evidence for transient pituitary desensitization after GRF stimulation.

Y Arsenijevic et al.

Endocrinology, 121(4), 1487-1496 (1987-10-01)

The ability of human (h)GRF-(1-29)NH2 to stimulate GH secretion was studied in cannulated adult rats. In order to suppress endogenous GRF secretion and the inhibitory action of hypothalamic somatostatin (SRIF), rats were anesthetized with sodium pentobarbital. Intravenous administration of hGRF-(1-29)NH2

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