PHD Finger Protein 21A (PHF21A) Antibody (Biotin)

Este producto es parte de PHF - PHD finger protein
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169€ (20 µg)

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935106861
info@markelab.com
name
PHD Finger Protein 21A (PHF21A) Antibody (Biotin)
category
Primary Antibodies
provider
Abbexa
reference
abx317094
tested applications
ELISA

Description

PHF21A Antibody (Biotin) is a Rabbit Polyclonal against PHF21A conjugated to Biotin.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
PHD Finger Protein 21A (PHF21A)
Host
Rabbit
Reactivity
Human
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Biotin
Isotype
IgG
Purity
> 95%
Purification
Purified by Protein G.
Size 1
20 µg
Size 2
50 µg
Size 3
100 µg
Size 4
200 µg
Size 5
1 mg
Form
Liquid
Tested Applications
ELISA
Buffer
0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q96BD5
Gene ID
51317
NCBI Accession
NP_001095272.1, NM_001101802.1
OMIM
608325
Alias
BHC80, BM-006, IDDBCS, NEDMS,BHC80a
Background
Antibody anti-PHF21A
Status
RUO

Descripción

PHF21A is a PHD finger-containing protein involved in chromatin remodeling and transcriptional repression through its interactions with histone modifications. It is a component of the BHC complex, where it facilitates histone deacetylation and demethylation to suppress gene expression. PHF21A plays an essential role in neural development, where it regulates genes involved in neuronal differentiation, synaptic plasticity, and brain formation. It binds to unmethylated CpG islands and recruits chromatin modifiers to maintain gene silencing in a tissue-specific manner. Dysregulation or mutations in PHF21A are associated with neurodevelopmental disorders, including intellectual disability and Potocki-Shaffer syndrome, which manifest as craniofacial abnormalities and cognitive impairments. Knockout studies reveal disrupted neuronal differentiation, altered gene silencing, and developmental defects, highlighting its role in transcriptional repression, neurodevelopment, and chromatin regulation.

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