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K1731 rabbit pAb

CAT: 0855-ES15368-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES15368-01Size:50 µL
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UniProt
Q9C0D2
Swiss Prot
Q9C0D2
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human K1731 AA range: 208-258
Clonality
Polyclonal
Source
Rabbit
Applications
IHC; IF
Concentration
1 mg/ml
Dilution
IHC-p 1: 50-200
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome . Cytoplasm, cytoskeleton, spindle . Cytoplasm, cytoskeleton . Associates with both of the converted centrioles during G1 but becomes more enriched at the newly formed daughter (or unconverted) centrioles during S, G2, and early M phases (PubMed:25131205, PubMed:32060285) . In early S phase, localized at the procentriolar microtubule wall and enriched at the proximal ends of the centrioles in CENPJ- and CEP135-dependent manner (PubMed:27185865) . Colocalizes with SASS6 and CEP250 proteins (PubMed:25131205) . Colocalizes with CEP135 and CEP192 at the centrosomes (PubMed:27185865) . Associates with interphase microtubules and mitotic spindles (PubMed:
Gene ID (Human)
85459

UniProtKB · Q9C0D2

Centrosomal protein of 295 kDa

CE295_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9C0D2
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CEP295
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
C9J5H9, C9JQY8, Q8N7L4, Q8N919, Q8N9B0, Q96LT8
Protein keywords

Coding sequence diversity

Alternative splicing

Biological process

Cilium biogenesis/degradation

Domain

Coiled coil

Cellular component

CytoplasmCytoskeleton

Disease

Disease variantDwarfismIntellectual disability

PTM

Phosphoprotein

Technical term

Proteomics identificationReference proteome

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