Anti-ACY1 Antibody

$99.00$319.00

Reactivity: Human,Mouse
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-ACY1 Antibody (CSB-PA860799ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

N-acyl-L-amino-acid amidohydrolase Antibody,ACY-1 Antibody,ACY1 Antibody

More alternative names for the antibody
ACY 1 antibody|ACY-1 antibody|Acy1 antibody|ACY1_HUMAN antibody|ACY1D antibody|ACYLASE antibody|Acylase I antibody|Aminoacylase-1 antibody|EC 3.5.1.14 antibody|epididymis secretory protein Li 5 antibody|HEL-S-5 antibody|N acyl L amino acid amidohydrolase antibody|N-acyl-L-amino-acid amidohydrolase antibody|OTTHUMP00000212459 antibody|OTTHUMP00000212462 antibody|OTTHUMP00000212463 antibody|OTTHUMP00000212464 antibody|OTTHUMP00000212465 antibody
Anti-Aminoacylase 1 antibody (ab54960)
Close sc-271705|sc-271019|sc-374298|

Recommended applications: ELISA, WB, IHC

Recommended dilution: Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-ACY1 Antibody

Catalogue No.

CSB-PA860799ESR1HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Aminoacylase-1 protein (1-408AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

45 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:95( Human), Omim:104620( Human), SwissProt:Q03154( Human), Unigene:334707( Human)

Protein function

Involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). .

Protein tissue specificity

Expression is highest in kidney, strong in brain and weaker in placenta and spleen. .

Involvement in disease

Aminoacylase-1 deficiency (ACY1D) [MIM:609924]: An enzymatic deficiency resulting in encephalopathy, unspecific psychomotor delay, psychomotor delay with atrophy of the vermis and syringomyelia, marked muscular hypotonia or normal clinical features. Epileptic seizures are a frequent feature. All affected individuals exhibit markedly increased urinary excretion of several N-acetylated amino acids. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the peptidase M20A family.

Protein cellular localization

Cytoplasm.

Research area

All research areas>Signaling Intermediates>Aminoacylase
(View all antibody categories related to Signaling Intermediates)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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