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PHKA1 Rabbit Polyclonal Antibody (Biotin)

CAT: 0013-GTR18340631Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18340631Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
PHKA1 Rabbit Polyclonal Antibody (Biotin)
Product Name Alternative
PHKA
UniProt
P46020
Immunogen
The immunogen for Anti-PHKA1 antibody is: synthetic peptide directed towards the C-terminal of Human KPB1
Clonality
Polyclonal
Conjugation
Biotin
Sequence
Synthetic peptide located within the following region: KQSPGTSMTPSSGSFPSAYDQQSSKDSRQGQWQRRRRLDGALNRVPVGFY
Field of Research
Signal Transduction
Purification
Affinity purified
Form
Liquid. Purified antibody supplied in 1x PBS buffer.
Molecular Weight
126 kDa
Storage Conditions
All conjugated antibodies should be stored in light-protected vials or covered with a light protecting material (i.e. aluminum foil) . Conjugated antibodies are stable for at least 12 months at 4C. If longer storage is desired (24 months), conjugates may be diluted with up to 50% glycerol and stored at -2°C to -8°C. Freezing and thawing conjugated antibodies will compromise enzyme activity as well as antibody binding.
Notes
For research use only.
Prediction Reactivity
Human
Tested Applications
WB
Host or Source
Rabbit
Preservative
Liquid. Purified antibody supplied in 1x PBS buffer.

UniProtKB · P46020

Phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform

KPB1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P46020
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
PHKA1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
Phosphorylase kinase alpha M subunit
EC number
—
Processing
—
Secondary accessions
B7ZL05, B7ZL07, Q2M3D7
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Molecular function

Calmodulin-bindingMuscle protein

Biological process

Carbohydrate metabolismGlycogen metabolism

Cellular component

Cell membraneMembrane

Disease

Disease variantGlycogen storage disease

PTM

LipoproteinPhosphoproteinPrenylation

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