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CEP250 Rabbit Polyclonal Antibody (APC)

CAT: 0013-GTR18543311Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18543311Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Anti-CEP250 Antibody. Tested in ELISA, Flow Cytometry, IHC, WB applications. This antibody reacts with Human, Mouse, Rat.
Product Name Alternative
250 kDa centrosomal protein, C NAP1, Centrosomal protein 2, centrosomal protein 250kDa, CEP2, CEP250, CNAP1, C-NAP1
UniProt
Q9BV73
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins.
Immunogen
E.coli-derived human CEP250 recombinant protein (Position: Q563-K853) .
Target
Centrosome-associated protein CEP250
Clonality
Polyclonal
Conjugation
APC
Field of Research
Cancer Biology, Cardiovascular Research, Cell Biology
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
25503 Da
Storage Conditions
At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
Rabbit IgG

UniProtKB · Q9BV73

Centrosome-associated protein CEP250

CP250_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9BV73
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CEP250
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
E1P5Q3, O14812, O60588, Q9H450
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Biological process

Cell cycleCilium biogenesis/degradation

Cellular component

Cell projectionCiliumCytoplasmCytoskeleton

Domain

Coiled coil

Disease

Cone-rod dystrophyDeafnessDisease variant

PTM

Phosphoprotein

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