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Anti-EYA4 Antibody

品牌：Antibodies

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规格：100µg

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Anti-EYA4 Antibody

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Overview

Name:	Anti-EYA4 Antibody See all EYA4 primary antibodies
Description:	Goat polyclonal antibody to EYA4.
Applications:	ELISA, IHC
Reactivity:	Human
Immunogen:	Synthetic peptide corresponding to Human EYA4 (N terminal).
Sequence:	EDSQDLNEQSVKKTC
Host:	Goat
Clonality:	Polyclonal
Isotype:	IgG
Conjugate:	Unconjugated
Purification:	Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Concentration:	100 μg at 0.5 mg/ml.
Product Form:	Liquid
Formulation:	Supplied in Tris Buffered Saline, pH 7.30, with 0.02% Sodium Azide and 0.5% BSA.
Storage:	Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

Target

Function:	Tyrosine phosphatase that specifically dephosphorylates 'Tyr-142' of histone H2AX (H2AXY142ph). 'Tyr-142' phosphorylation of histone H2AX plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress. Promotes efficient DNA repair by dephosphorylating H2AX, promoting the recruitment of DNA repair complexes containing MDC1. Its function as histone phosphatase probably explains its role in transcription regulation during organogenesis. May be involved in development of the eye (By similarity).
Tissue Specificity:	Highly expressed in heart and skeletal muscle.
Involvement in Disease:	Deafness, autosomal dominant, 10: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. Cardiomyopathy, dilated 1J: A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. CMD1J is characterized by the association of sensorineural hearing loss and dilated cardiomyopathy in the absence of other anomalies.
Sequence Similarities:	Belongs to the HAD-like hydrolase superfamily. EYA family.
Cellular Location:	Cytoplasm. Nucleus.
Database Links:	Entrez Gene: 2070?Human Omim: 603550?Human SwissProt: O95677?Human Unigene: 596680?Human
Synonyms:	CMD1J Antibody Deafness, autosomal dominant 10 Antibody DFNA 10 Antibody DFNA10 Antibody dJ78N10.1 (eyes absent (Drosophila) homolog 4) Antibody dJ78N10.1 (eyes absent) Antibody EYA 4 Antibody EYA4 Antibody EYA4_HUMAN Antibody Eyes absent 4 Antibody Eyes absent homolog 4 Antibody Eyes absent homolog 4 (Drosophila) Antibody HGNC:3522 Antibody OTTHUMP00000040267 Antibody
Information:	Target information shown above is from the UniProt Consortium.