Products for Research Use Only

KIDINS220 Antibody

CAT: 0013-GTR17881921-01Size: 50 µgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0013-GTR17881921-01Size:50 µg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
This KIDINS220 Antibody is an unconjugated polyclonal product. It tagets KIDINS220 using a Recombinant Human Kinase D-interacting substrate of 220 kDa protein (1077-1370AA) as the immunogen. This antibody is suitable for ELISA, IF, IHC, WB. Purification: >95%, Protein G purified.
Product Name Alternative
Ankyrin repeat-rich membrane-spanning protein antibody; arms antibody; KDIS_HUMAN antibody; kidins220 antibody; Kinase D interacting substance of 220 kDa antibody; Kinase D-interacting substrate of 220 kDa antibody; rgd 619949 antibody
UniProt
Q9ULH0
Reactivity
Human
Immunogen
Recombinant Human Kinase D-interacting substrate of 220 kDa protein (1077-1370AA)
Target
KIDINS220
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
>95%, Protein G purified
Dilution
WB:1:500-5000, IHC-P:1:20-200, IF:1:50-200
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
ELISA, IF, IHC, WB
Host or Source
Rabbit
Preservative
Preservative: 0.03% Proclin 300. Constituents: 50% Glycerol
Isotype
IgG

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

Alternative Products