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AB95814

Anti-PDE3B antibody [SMCP3B]

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(3 Publications)

Rat Monoclonal PDE3B antibody. Suitable for WB and reacts with Mouse samples. Cited in 3 publications. Immunogen corresponding to Recombinant Fragment Protein within Mouse Pde3b aa 600 to C-terminus.

View Alternative Names

CGIPDE1, Cyclic GMP-inhibited phosphodiesterase B, CGI-PDE B, Pde3b

1 Images
Western blot - Anti-PDE3B antibody [SMCP3B] (AB95814)
  • WB

Unknown

Western blot - Anti-PDE3B antibody [SMCP3B] (AB95814)

Run on a 3-8% Tris-Acetate gel.

All lanes:

Western blot - Anti-PDE3B antibody [SMCP3B] (ab95814) at 2 µg/mL

Lane 1:

Mouse heart cell lysate

Lane 2:

Mouse lymph node cell lysate

Secondary

All lanes:

Anti-Rat IgG HRP

Predicted band size: 124 kDa

false

Key facts

Host species

Rat

Clonality

Monoclonal

Clone number

SMCP3B

Isotype

IgG2a

Light chain type

kappa

Carrier free

No

Reacts with

Mouse

Applications

WB

applications

Immunogen

Recombinant Fragment Protein within Mouse Pde3b aa 600 to C-terminus. The exact immunogen used to generate this antibody is proprietary information.

Q61409

Specificity

ab95814 is specific to PDE3B. It does not react with PDE3A.

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "WB-species-checked": "notRecommended", "WB-species-dilution-info": "1-5 µg/mL", "WB-species-notes": "<p></p>" }, "Mouse": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1-5 µg/mL", "WB-species-notes": "<p></p>" } } }

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein G
Storage buffer
pH: 7.2 Preservative: 0.09% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

PDE3B also known as cGMP-inhibited phosphodiesterase B is an enzyme with a role in cyclic nucleotide signaling. It possesses a molecular mass of approximately 133 kDa. PDE3B predominantly gets expressed in adipose tissue liver and to some extent in the heart. It breaks down cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) which play key roles in cellular signaling. By hydrolyzing these cyclic nucleotides into their non-cyclic forms PDE3B regulates intracellular levels of these molecules.
Biological function summary

In adipose tissue and liver PDE3B modulates lipogenesis and lipolysis which are vital processes for energy balance. This enzyme interacts with signaling pathways that involve protein kinase A (PKA) and insulin signaling. PDE3B operates as part of larger protein complexes and influences the metabolic rate by regulating the availability of the cAMP for phosphorylation reactions. The activity of PDE3B links closely to the control of energy homeostasis due to its regulatory function on lipid metabolism.

Pathways

PDE3B is integral to the insulin signaling pathway and adiponectin signaling pathway both important in glucose and lipid homeostasis. Within these pathways it functions alongside proteins like AKT and PKA where its activity modulates their signaling efficiency. By controlling the balance of cAMP PDE3B influences signaling cascades that are important for the adaptive cellular responses to hormones and nutrients.

PDE3B connects to conditions such as obesity and type 2 diabetes due to its involvement in energy homeostasis and lipid metabolism. In type 2 diabetes the dysregulation of PDE3B activity affects insulin signaling and glucose uptake. Additionally in the context of obesity PDE3B activity shifts the balance of lipolysis and lipogenesis influencing adipose tissue mass and function. Proteins such as insulin receptors and PKA become closely tied to PDE3B in these disorders highlighting its role in metabolic disease mechanisms.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Cyclic nucleotide phosphodiesterase with a dual-specificity for the second messengers cAMP and cGMP, which are key regulators of many important physiological processes (PubMed : 10454575). Regulates angiogenesis by inhibiting the cAMP-dependent guanine nucleotide exchange factor RAPGEF3 and downstream phosphatidylinositol 3-kinase gamma-mediated signaling (By similarity). Controls cardiac contractility by reducing cAMP concentration in cardiocytes (PubMed : 15294162).
See full target information Pde3b

Publications (3)

Recent publications for all applications. Explore the full list and refine your search

Physiological reports 12:e70089 PubMed39435735

2024

Pde3a and Pde3b regulation of murine pulmonary artery smooth muscle cell growth and metabolism.

Applications

Unspecified application

Species

Unspecified reactive species

Paulina N Krause,Gabrielle McGeorge,Jennifer L McPeek,Sidra Khalid,Leif D Nelin,Yusen Liu,Bernadette Chen

Obesity (Silver Spring, Md.) 31:1859-1870 PubMed37254272

2023

An Artemisia scoparia extract attenuates glucocorticoid-induced lipolysis in adipocytes.

Applications

Unspecified application

Species

Unspecified reactive species

Innocence Harvey,Jacqueline M Stephens

The Biochemical journal 456:463-73 PubMed24007532

2013

Regulatory T-cells and cAMP suppress effector T-cells independently of PKA-CREM/ICER: a potential role for Epac.

Applications

Unspecified application

Species

Unspecified reactive species

Amanda G Vang,William Housley,Hongli Dong,Chaitali Basole,Shlomo Z Ben-Sasson,Barbara E Kream,Paul M Epstein,Robert B Clark,Stefan Brocke
View all publications

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