Products for Research Use Only

KIDINS220 Rabbit Polyclonal Antibody

CAT: 0013-GTR18319339-01Size: 30 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18319339-01Size:30 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
The KIDINS220 Antibody is suitable for WB. It is a Polyclonal, Unconjugated antibody which raised against KLH-conjugated synthetic peptide encompassing a sequence within the C-terminal region of human KIDINS220. The exact sequence is proprietary. Purification: The antibody was purified by immunogen affinity chromatography.
Product Name Alternative
ARMS; KIAA1250; Kinase D-interacting substrate of 220 kDa; Ankyrin repeat-rich membrane-spanning protein
UniProt
Q9ULH0
Reactivity
Human
Immunogen
KLH-conjugated synthetic peptide encompassing a sequence within the C-terminal region of human KIDINS220. The exact sequence is proprietary.
Target
KIDINS220
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
The antibody was purified by immunogen affinity chromatography.
Dilution
WB (1/500 - 1/1000)
Form
Liquid
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
0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Entrez
57498

UniProtKB · Q9ULH0

Kinase D-interacting substrate of 220 kDa

KDIS_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9ULH0
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
KIDINS220
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A1L4N4, Q4VC08, Q6MZU2, Q9H889, Q9H9E4, Q9NT37, Q9UF42
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Domain

ANK repeatRepeatTransmembraneTransmembrane helix

Disease

Disease variantHereditary spastic paraplegiaIntellectual disabilityNeurodegenerationObesity

Cellular component

EndosomeMembrane

Biological process

Neurogenesis

PTM

Phosphoprotein