Human Adenylate Cyclase Type 8 (ADCY8) Protein

Este producto es parte de ADCY - Adenylate Cyclase Type
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247€ (10 µg)

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935106861
info@markelab.com
name
Human Adenylate Cyclase Type 8 (ADCY8) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx167169
tested applications
WB, SDS-PAGE

Description

Adenylate Cyclase Type 8 Protein is a recombinant Human protein expressed in E. coli.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryProteins and Peptides
Immunogen TargetAdenylate Cyclase Type 8 (ADCY8)
HostE. coli
OriginHuman
ConjugationUnconjugated
Observed MWMolecular Weight: Calculated MW: 45.3 kDa Observed MW (SDS-PAGE): 48 kDa Concentration: Prior to lyophilization: 200 µg/ml Sequence Fragment: Lys234-Glu371 Tag: N-terminal His tag and GST tag
ExpressionRecombinant
Purity> 95%
Size 110 µg
Size 250 µg
Size 3100 µg
Size 4200 µg
Size 5500 µg
FormLyophilized Reconstitute in ddH2O to a concentration of 0.1-1.0 mg/ml. Do not vortex.
Tested ApplicationsWB, SDS-PAGE
BufferPrior to lyophilization: 100 mM NaHCO<sub>3</sub>, 500 mM NaCl, pH 8.3, containing 1 mM EDTA, 1 mM DTT, 0.01% Sarcosyl, 5% Trehalose and Proclin-300.
AvailabilityShipped within 5-7 working days.
StorageStore at 2-8 °C for up to one month. Store at -80 °C for up to one year. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDP40145
Gene ID114
OMIM103070
AliasAC8,ADCY3,HBAC1
BackgroundProtein ADCY8
StatusRUO
NoteThis product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

ADCY8 is a calcium/calmodulin-activated enzyme predominantly expressed in the brain, particularly in regions involved in synaptic plasticity and memory formation. It plays a key role in generating cAMP in response to elevated calcium levels, thereby regulating neuronal excitability and synaptic strength. ADCY8 is involved in processes such as learning, memory, and mood regulation. Dysregulation of ADCY8 has been linked to neurological disorders, including depression and cognitive decline, due to impaired calcium-dependent cAMP signaling.

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