Anti-DCUN1D4 antibody
英文名称 | DCUN1D4 |
中文名称 | DCN1样蛋白4抗体 |
别 名 | DCN1 like protein 4; DCN1, defective in cullin neddylation 1, domain containing 4 (S. cerevisiae); DCN1, defective in cullin neddylation 1, domain containing 4; DCN1-like protein 4; DCNL4_HUMAN; DCUN1 domain containing protein 4; DCUN1 domain-containing protein 4; DCUN1D 4; Dcun1d4; Defective in cullin neddylation protein 1-like protein 4; KIAA0276. |
DATASHEET
Host:Rabbit
Target Protein:DCUN1D4
IR:Immunogen Range:201-292/292
Clonality:Polyclonal
Isotype:IgG
Entrez Gene:23142
Swiss Prot:Q92564
Source:KLH conjugated synthetic peptide derived from human DCUN1D4:201-292/292
Purification:affinity purified by Protein A
Storage:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
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.
Size:100ul
Concentration:1mg/ml
Applications:ELISA(1:5000-10000)
IHC-P(1:100-500)
IHC-F(1:100-500)
ICC(1:100-500)
IF(1:100-500)
Cross Reactive Species:Human
Mouse
Rat
Dog
Pig
Cow
Horse
Sheep
.
For research use only. Not intended for diagnostic or therapeutic use.
好评度