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FBXW7 Antibody

CAT: 0864-A55971-50ULSize: 50 μLDry Ice: NoHazardous: No
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CAT#:0864-A55971-50ULSize:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
AGO, Archipelago, Archipelago homolog, Archipelago, Drosophila, homolog of, CDC4, CDC4, S.cerevisiae, homolog of, DKFZp686F23254, F box and WD 40 domain protein 7 (archipelago homolog, Drosophila) , F box and WD 40 domain protein 7, F box and WD repeat domain containing 7, F box protein FBW7, F box protein FBX30, F box protein SEL 10, F box protein SEL10, F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase, F-box and WD-40 domain-containing protein 7, F-box protein FBX30, F-box/WD repeat-containing protein 7, FBW6, FBW7, FBX30, FBXO30, FBXW6, FBXW7, FBXW7_HUMAN, FLJ16457, hAgo, hCdc4, Homolog of C elegans sel 10, Homolog of C.elegans sel10, SEL 10, SEL-10, SEL10
UniProt
Q969H0
Host
Rabbit
Antigen Species
Human
Reactivity
Human, Mouse
Target Antigen
Fusion protein of Human FBXW7
Target
FBXW7
Clonality
Polyclonal
Conjugation
Non-conjugated
Applications
ELISA, IHC, ELISA:1:2000-1:5000, IHC:1:50-1:200
Field of Research
Cell Biology
Purification Method
Antigen affinity purified
Form
Liquid
Buffer
PBS, 0.05% sodium azide, 40% glycerol, pH 7.4.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · Q969H0

F-box/WD repeat-containing protein 7

FBXW7_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q969H0
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
FBXW7
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
B7ZLP9, Q68DR0, Q96A16, Q96LE0, Q96RI2, Q9NUX6
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Biological process

Biological rhythmsDNA damageDNA repairHost-virus interactionUbl conjugation pathway

Cellular component

ChromosomeCytoplasmNucleus

Disease

Disease variantIntellectual disability

PTM

PhosphoproteinUbl conjugation

Domain

RepeatWD repeat

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