Rabbit Polyclonal Anti-EPG5 antibody (STJ98818)

$99.00$319.00

Reactivity: Human
Applications: IHC-P, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Rabbit Polyclonal Anti-EPG5 antibody (STJ98818)

Supplier: St John’s Laboratory Ltd.

Recommended applications: IHC-P, ELISA

Recommended dilution: IHC-P 1:50-300; ELISA 1:5000-20000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody

Expand

|Ectopic P granules autophagy protein 5 homolog (C. elegans) antibody|Ectopic P granules protein 5 homolog antibody|Epg5 antibody|EPG5_HUMAN antibody|HEEW1 antibody|hEPG5 antibody|KIAA1632 antibody|Anti-EPG5 antibody (ab122186)
SCBT cat No:

Name

Anti-EPG5 antibody

Catalogue No.

STJ98818

Reactivity

Human

Specificity

Anti-EPG5 antibody detects endogenous EPG5.

Immunogen

Synthetic peptide from human protein at AA range: 141-190.

Host

Rabbit

Applications

IHC-P, ELISA

Recommended dilution

IHC-P 1:50-300; ELISA 1:5000-20000

Clonality

Polyclonal

Conjugation

Unconjugated

Isotype

IgG

Formulation

Anti-EPG5 antibody was tube-contained in PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.

Concentration

1 mg/ml

Purification

Anti-EPG5 antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Ectopic P granules autophagy protein 5 homolog (C. elegans) antibody, Ectopic P granules protein 5 homolog antibody, Epg5 antibody, EPG5_HUMAN antibody, HEEW1 antibody, hEPG5 antibody, KIAA1632 antibody

Database links

UniProt/Swiss-Prot:Q9HCE0

Protein function

Involved in autophagy. May play a role in a late step of autophagy, such as clearance of autophagosomal cargo. .

Involvement in disease

Vici syndrome (VICIS) [MIM:242840]: A rare congenital multisystem disorder characterized by agenesis of the corpus callosum, cataracts, pigmentary defects, progressive cardiomyopathy, and variable immunodeficiency. Affected individuals also have profound psychomotor retardation and hypotonia due to a myopathy. . Note=The disease is caused by mutations affecting the gene represented in this entry. Affected individuals show homozygosity or compound heterozygosity for truncating mutations, aberrant splicing and/or missense mutations. Parental studies suggest recessive inheritance with no carrier manifestation (PubMed:23222957). .

Protein sequence and domain

Belongs to the EPG5 family.

Note

AntibodyPlus can customize Anti-EPG5 antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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