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Alpha Dystroglycan Rabbit Polyclonal Antibody

CAT: 0013-GTR17724066-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR17724066-01Size:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Alpha Dystroglycan Rabbit Polyclonal Antibody
Product Name Alternative
156DAG; A3a; AGRNR; DAG; LGMDR16; MDDGA9; MDDGC7; MDDGC9; D9Wsu13e; DG; Dp427; Dp71; DAG1_HUMAN; DAG1; Dystroglycan; Dystrophin-associated glycoprotein 1; DAG1_MOUSE; dystroglycan 1; dystroglycan 1 (dystrophin-associated glycoprotein 1) ; alpha-dystroglycan; dystrophin-associated glycoprotein-1; beta-dystroglycan
UniProt
Q14118
Reactivity
Mouse, Rat
Immunogen
KLH conjugated synthetic peptide derived from human DAG1 (451-550/895aa)
Target
DAG1
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Actin Binding Proteins, Cell Biology, Neurogenesis, Neuroscience
Purification
Affinity purified by Protein A
Concentration
1mg/ml
Dilution
IHC-P=1:100-500, IHC-F=1:100-500, IF=1:200-800
Form
Liquid
Molecular Weight
98 kDa
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.
Prediction Reactivity
Canine, Equine, Gallus, Human, Porcine, Rabbit
Tested Applications
IF, IHC-Fr, IHC-P
Host or Source
Rabbit
Preservative
0.01M TBS (pH7.4) with 1% rAlbumin, 0.02% Proclin300 and 50% Glycerol.
Isotype
IgG

UniProtKB · Q14118

Dystroglycan 1

DAG1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q14118
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
DAG1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
A8K6M7, Q969J9
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

Autocatalytic cleavageDisulfide bondGlycoproteinPhosphoprotein

Cellular component

Basement membraneCell membraneCytoplasmCytoskeletonExtracellular matrixMembraneNucleusPostsynaptic cell membraneSecretedSynapse

Disease

Congenital muscular dystrophyDisease variantDystroglycanopathyLimb-girdle muscular dystrophyLissencephaly

Molecular function

Host cell receptor for virus entryReceptor

Biological process

Host-virus interaction

Domain

SignalTransmembraneTransmembrane helix

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