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Specifications
- Antibody Type:Primary
- Antigen Name:AMPD3
- Clonality:Polyclonal
- Conjugation:Alexa Fluor® 750
- Host:Rabbit
- ImmunoChemistry:Yes
- ImmunoFluorescence:Yes
- Isotype:IgG
- Reactivity:Human,Rat,Mouse
- Western Blot:Yes
- Size:100 µl
- Environmentally Preferable:
- Epitope:21-120/767
- Form:Liquid
- Gene ID:272
- Antigen Synonyms:Erythrocyte type AMP deaminase|AMP deaminase 3|Erythrocyte AMP deaminase|Ampd3|Myoadenylate deaminase|Adenosine monophosphate deaminase isoform E|AMPD3_HUMAN|Erythrocyte specic AMP deaminase|AMP aminohydrolase|Adenosine monophosphate deaminase 3|AMP deaminase isoform E
- Modification:Unmodified
- Storage Buffer:Aqueous buffered solution containing 0.01 M TBS (pH 7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
- Storage Temperature:Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Concentration:1 µg/µl
- Shipping Temperature:4 °C
- Immunogen:KLH conjugated synthetic peptide derived from human AMPD3
- Purification:Purified by Protein A
- Cat. No.:76110-732
- Packaging:Vial
Specifications
About this item
AMP deaminase plays a critical role in energy metabolism. Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is 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.
Type: Primary
Antigen: AMPD3
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 750
Public Immunogen Range: 21-120/767
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat