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  3. Cerebellin

Cerebellin is a neuromodulatory peptide widely distributed in the central nervous system.

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Cerebellin Chemical Structure

Cerebellin Chemical Structure

CAS No. : 94071-26-8

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Cerebellin Related Antibodies

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  • Biological Activity

  • Protocol

  • Purity & Documentation

  • References

  • Customer Review

Description

Cerebellin is a neuromodulatory peptide widely distributed in the central nervous system.

In Vitro

Cerebellin concentration-dependently (from 1 to 100 nM) increases norepinephrine (but not epinephrine) and cyclic-AMP production by adrenomedullary tissue in vitro[1].

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

Cerebellin Related Antibodies
In Vivo

Cerebellin potently stimulates norepinephrine release by rat adrenal medulla, acting through adenylate-cyclase/PKA-coupled receptors, and enhances adrenocortical steroid secretion in vivo (i.e. when the integrity of adrenal gland is preserved) through an indirect paracrine mechanism involving the release of medullary catecholamines[1]. Cerebellin reduces plasma insulin levels in rats after 1 and 2 h. Cerebellin decreases insulin secretion from isolated rat pancreatic islets at high (11 mM), but not at low (3.33 mM) glucose concentration. Cerebellin inhibits stimulated insulin secretion from clonal rat insulinoma (INS-1) cells, reduces forskolin-induced production of cAMP and intracellular calcium concentration[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Molecular Weight

1632.78

Formula

C69H113N23O23
CAS No.
Sequence

Ser-Gly-Ser-Ala-Lys-Val-Ala-Phe-Ser-Ala-Ile-Arg-Ser-Thr-Asn-His
Sequence Shortening

SGSAKVAFSAIRSTNH
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

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 (<0) 1.  Try to dissolve the peptide in water first.
2.  If water fails, add NH4OH (<50 μL).
3.  If the peptide still does not dissolve, add DMSO (50-100 μL) to solubilize the peptide.
Positive (>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.
Purity & Documentation
References
Kinase Assay
[1]

Some adrenomedullary samples are incubated with 10 μM H89, U-73122 or calphostin-C alone or in the presence of 0.1 μM cerebellin. When cyclic-AMP production is assayed, 100 μM 3-isobutyl-1-methylxanthine is added to prevent cyclic-AMP metabolism by phosphodiesterases. Incubation is carried out for 60 min (aldosterone or corticosterone production), 30 min (catecholamine production) or 10 min (cyclic-AMP production) in a shaking bath at 37°C in an atmosphere of 95% air -5% CO2. At the end of the experiments, the incubation tubes are centrifuged at 4°C, and media are collected and kept frozen at -80°C[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Administration
[2]

Rats[2]

Adult female Wistar rats (180–190 g body weight, 8–12 weeks of age) are injected daily with 0.2 mL of 0.9% NaCl (s.c.) for 14 days. On day 15, animals receive s.c. injections of 0.2 mL of 0.9% NaCl (control groups), while experimental groups are treated with 0.5 or 1.5 nmol/100 g body weight Cerebellin0.5 or 1.5 nmol/100 g body weight Cerebellin. Rats are decapitated 60 or 120 min after injection. Blood is collected into ice-cold tubes containing EDTA (1 mg/mL) and analyzed for the concentration of glucose. Plasma is separated and stored at −80 °C for the determination of the insulin and glucagon concentration[2].

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

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Cerebellin94071-26-8OthersInhibitorinhibitorinhibit

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