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KIF1B antibody

CAT: 0710-FNab04555Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0710-FNab04555Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Background
This gene encodes a motor protein that transports mitochondria and synaptic vesicle precursors. Mutations in this gene cause Charcot-Marie-Tooth disease, type 2A1.
Synonyms
Kinesin-like protein KIF1B (Klp) |KIF1B|KIAA0591|KIAA1448
Gene ID
23095
UniProt
O60333
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Kinesin family member 1B
Target
KIF1B
Clonality
Polyclonal
Isotype
IgG
Applications
ELISA, WB, IHC
Field of Research
Cell Division and Proliferation, Developmental biology
Purification
Immunogen affinity purified
Dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:200
Purity
≥95% as determined by SDS-PAGE
Form
Liquid
Molecular Weight
200 kDa
Shipping Conditions
4°C with ice bag
Storage Conditions
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Tested Applications
ELISA, WB, IHC

UniProtKB · O60333

Kinesin-like protein KIF1B

KIF1B_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O60333
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
KIF1B
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
Klp
EC number
5.6.1.3
Processing
—
Secondary accessions
A6NFS8, A6NKQ4, Q4VXC3, Q4VXC4, Q4VXC5, Q4VXC6, Q96Q94, Q9BV80, Q9P280
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationPhosphoprotein

Coding sequence diversity

Alternative splicing

Biological process

Apoptosis

Ligand

ATP-bindingNucleotide-binding

Disease

Charcot-Marie-Tooth diseaseDisease variantNeurodegenerationNeuropathy

Domain

Coiled coil

Cellular component

CytoplasmCytoplasmic vesicleCytoskeletonMembraneMicrotubuleMitochondrionSynapse

Molecular function

IsomeraseMotor protein

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