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AMPD2 polyclonal antibody

CAT: 0013-GTR18296695-02Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18296695-02Size:100 µL
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Description
AMPD2 polyclonal antibody
Product Name Alternative
AMPD2; PCH9; SPG63
UniProt
Q01433
Reactivity
Human, Rat
Immunogen
Recombinant fusion protein of human AMPD2 (NP_631895.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Metabolism Research
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE) .
Concentration
1mg/ml
Dilution
WB,1:500 - 1:2000
Form
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH 7.2
Molecular Weight
Refer to figures
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
WB
Host or Source
Rabbit
Preservative
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH 7.2

UniProtKB · Q01433

AMP deaminase 2

AMPD2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q01433
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
AMPD2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
3.5.4.6
Processing
—
Secondary accessions
A0A5F9UK94, B4DK50, B4DZI5, E9PNG0, Q14856, Q14857, Q16686, Q16687, Q16688, Q16729, Q5T693, Q5T695, Q96IA1, Q9UDX8, Q9UDX9, Q9UMU4
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Disease

Disease variantHereditary spastic paraplegiaNeurodegeneration

Molecular function

Hydrolase

Ligand

Metal-bindingZinc

PTM

MethylationPhosphoprotein

Biological process

Nucleotide metabolism

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