PHD Finger Protein 2 (PHF2) Antibody

Este producto es parte de PHF - PHD finger protein
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364€ (100 µg)

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935106861
info@markelab.com
name
PHD Finger Protein 2 (PHF2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx236384
tested applications
ELISA, WB, IHC, IP

Description

PHF2 Antibody is a Rabbit Polyclonal against PHF2.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
PHD Finger Protein 2 (PHF2)
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1/200 - 1/1000, IHC: 1/20 - 1/200, IP: 1/500 - 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purity
≥ 95% (SDS-PAGE)
Purification
Purified by immunogen affinity chromatography.
Size 1
100 µg
Form
Liquid
Tested Applications
ELISA, WB, IHC, IP
Buffer
PBS, pH 7.3, with 0.02% sodium azide and 50% glycerol.
Availability
Shipped within 5-12 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
O75151
Gene ID
5253
OMIM
604351
Alias
CENP-35,GRC5, JHDM1E, KDM7C
Background
Antibody anti-PHF2
Status
RUO
Note
Concentration: 2 mg/ml - Validity: 12 months.

Descripción

PHF2 is a histone demethylase that specifically targets H3K9me2 to activate transcription by removing repressive methyl marks on histones. It serves as a transcriptional co-activator that regulates gene expression in response to metabolic and cellular stress signals. PHF2 is recruited to gene promoters through interactions with transcription factors and chromatin-associated proteins, promoting the activation of genes involved in lipid metabolism, gluconeogenesis, and inflammatory responses. It is expressed in metabolic tissues such as the liver, skeletal muscle, and adipose tissue, where it plays a role in energy homeostasis and inflammation control. Dysregulation of PHF2 is associated with metabolic diseases, including obesity, diabetes, and cancer, where its role in histone demethylation is disrupted. Knockdown studies reveal decreased transcriptional activation, impaired lipid metabolism, and abnormal inflammatory responses, highlighting its role in epigenetic regulation, metabolism, and cellular stress adaptation.

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