DCUN1D4 antibody (AA 161-270) (Cy5.5)
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- Target See all DCUN1D4 Antibodies
- DCUN1D4 (DCN1, Defective in Cullin Neddylation 1, Domain Containing 4 (DCUN1D4))
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Binding Specificity
- AA 161-270
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Reactivity
- Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This DCUN1D4 antibody is conjugated to Cy5.5
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Mouse
- Predicted Reactivity
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human DCUN1D4
- Isotype
- IgG
- Top Product
- Discover our top product DCUN1D4 Primary Antibody
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- Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- DCUN1D4 (DCN1, Defective in Cullin Neddylation 1, Domain Containing 4 (DCUN1D4))
- Alternative Name
- DCUN1D4 (DCUN1D4 Products)
- Synonyms
- RGD1310422 antibody, si:ch211-14g4.1 antibody, AI836376 antibody, DCN1-like protein 4 antibody, defective in cullin neddylation 1 domain containing 4 antibody, DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae) antibody, LOC100282616 antibody, LOC100283419 antibody, dcnl4 antibody, DCUN1D4 antibody, Dcun1d4 antibody, dcun1d4 antibody
- Background
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Synonyms: DCN1, defective in cullin neddylation 1, domain containing 4, DCN1 like protein 4, DCUN1 domain containing protein 4, DCUN1D 4, KIAA0276, DCNL4_HUMAN.
Background: The DCN1-like protein family is comprised of Dcun1D1, Dcun1D2, Dcun1D3, Dcun1D4 and Dcun1D5. The founding member, Dcun1D1, is involved in the malignant transformation of squamous cell lineage.Dcun1D4, (defective in cullin neddylation protein 1-like protein 4 or DCN1-like protein 4), also designated KIAA0276, exists as 2 isoforms as a result of alternative splicing and contains one DCUN1 domain. The gene encoding Dcun1D4 maps to chromosome 4, which houses nearly 6 % of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
- Gene ID
- 23142
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