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Western blot analysis in human placenta tissue lysate (35ug/lane). This demonstrates that the detected AMPD3 protein (arrow).
Western blot analysis in human placenta tissue lysates (35ug/lane).
Western blot analysis of anti-AMPD3 Antibody in mouse lung tissue lysates (35ug/lane)
Western blot analysis in human placenta tissue lysate (35ug/lane). This demonstrates that the detected AMPD3 protein (arrow).

AMPD3 Antibody

CATALOG NUMBER: 63-256

Clonality:
Polyclonal
Tested Applications:
WB
Host Species:
Rabbit
Species Reactivity:
Human, Mouse
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human, Mouse
Immunogen:
This AMPD3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 325-356 amino acids from the Central region of human AMPD3.
Conjugate:
Unconjugated
Tested Applications:
WB
Application Note:
For WB starting dilution is: 1:1000
Predicted Molecular Weight:
89 kDa
Purification:
This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis
Clonality:
Polyclonal
Isotype:
Rabbit Ig
physical-state:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Storage Conditions:
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Ncbi Official Symbol:
AMPD3
Additional Names:
AMP deaminase 3, AMP deaminase isoform E, Erythrocyte AMP deaminase, AMPD3
Protein Accession Number:
Q01432
Protein Gi Number:
399033
Ncbi Gene Id Number:
272
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
AMPD3 is a member of the AMP deaminase gene family. This protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. The protein is the erythrocyte (E) isoforms, whereas other family members isoforms predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency.
Background Reference 1:
Mahnke-Zizelman D.K., Eddy R.Biochim. Biophys. Acta 1306:75-92(1996)
Background Reference 2:
Yamada Y., Goto H., Wakamatsu N., Ogasawara N.Hum. Mutat. 17:78-78(2001)

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

63-256

List Size:
400 ul

List Price:

$495.00

Datasheet
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