Anti-AMPD3 Antibody

$99.00$319.00

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

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Rabbit Anti-AMPD3 Antibody (CSB-PA001682ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

AMP deaminase isoform E Antibody,Erythrocyte AMP deaminase Antibody,AMPD3 Antibody

More alternative names for the antibody
Adenosine monophosphate deaminase (isoform E) antibody|Adenosine monophosphate deaminase 3 antibody|AMP aminohydrolase antibody|AMP deaminase 3 antibody|AMP deaminase isoform E antibody|Ampd3 antibody|AMPD3_HUMAN antibody|Erythrocyte AMP deaminase antibody|Erythrocyte specific AMP deaminase antibody|Erythrocyte specific protein antibody|Erythrocyte type AMP deaminase antibody|Erythroid Marker antibody|Myoadenylate deaminase antibody|OTTHUMP00000230743 antibody|OTTHUMP00000230746 antibody|OTTHUMP00000230747 antibody|OTTHUMP00000230748 antibody|OTTHUMP00000230749 antibody
Anti-AMPD3 antibody [AMPD3/901] – BSA and Azide free (ab212413)
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Recommended applications: ELISA, WB, IHC

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

Recommended protocols: check protocols

Name

Anti-AMPD3 Antibody

Catalogue No.

CSB-PA001682ESR1HU

Reactivity

Human, Mouse

Immunogen

Recombinant human AMP deaminase 3 protein (1-260AA)

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

88 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:272( Human), Omim:102772( Human), SwissProt:Q01432( Human), Unigene:501890( Human)

Protein function

AMP deaminase plays a critical role in energy metabolism.

Involvement in disease

Adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE) [MIM:612874]: A metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the adenosine and AMP deaminases family.

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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