Metabolism Antibodies 2

AMPD1 Rabbit Polyclonal Antibody (CAB7876)

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SKU:
CAB7876
Product Type:
Antibody
Host Species:
Rabbit
Isotype:
IgG
Antibody Type:
Polyclonal Antibody
Research Area:
Metabolism
Reactivity:
Human, Mouse, Rat
Synonyms:
MAD, MADA, MMDD, AMPD1
Research Use:
Metabolism
Frequently bought together:

Description

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AMPD1 Antibody (CAB7876)

The AMPD1 Antibody (CAB7876) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody, produced in rabbits, exhibits high specificity and sensitivity for detecting AMP deaminase 1 in human samples. It has been extensively validated for use in Western blot applications, allowing for precise and reliable analysis of this crucial enzyme.AMP deaminase 1 plays a key role in maintaining cellular energy levels and regulating metabolic processes.

This antibody is validated for use in WB, ELISA applications and has demonstrated reactivity against Human, Mouse, Rat samples.

Product Name:AMPD1 Antibody
SKU:CAB7876
Size:20μL, 100μL
Reactivity:Human, Mouse, Rat
Conjugate:Unconjugated
Immunogen:Synthetic peptide. This information is considered to be commercially sensitive.
Sequence:MNVR IFYS VSQS PHSL LSLL FYCA ILES RISA TMPL FKLP AEEK QIDD AMRN FAEK VFAS EVKD EGGR QEIS PFDV DEIC PISH HEMQ AHIF HLET LSTS
Tested Applications:WB ELISA
Recommended Dilution:
WB1:500 - 1:2000
ELISARecommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Synonyms:MAD, MADA, MMDD, AMPD1
Positive Sample:HT-29, Mouse skeletal muscle, Mouse thymus, Mouse pancreas
Cellular Localization:Cytosol.
Calculated MW:86kDa
Observed MW:80kDa

Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.

Purification MethodAffinity purification
Gene ID270
RRIDAB_2768351
Buffer InformationStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol, preserved with proclin300 or sodium azide, pH 7.3.
Product ImageWestern blot analysis of various lysates using AMPD1 Rabbit pAb (CAB7876) at 1:500 dilution. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit (AbGn00021). Exposure time: 90s.
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