Western Blot: DKC1 Antibody (2W2V6) [NBP3-16405] - Western blot analysis of extracts of PC-3 cells, using DKC1 Rabbit mAb (NBP3-16405) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 ...read more
Immunohistochemistry-Paraffin: DKC1 Antibody (2W2V6) [NBP3-16405] - Immunohistochemistry of paraffin-embedded mouse testis using DKC1 Rabbit mAb (NBP3-16405) at dilution of 1:100 (40x lens).Perform microwave antigen ...read more
Western Blot: DKC1 Antibody (2W2V6) [NBP3-16405] - Western blot analysis of extracts of various cell lines, using DKC1 Rabbit mAb (NBP3-16405) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at ...read more
Immunohistochemistry-Paraffin: DKC1 Antibody (2W2V6) [NBP3-16405] - Immunohistochemistry of paraffin-embedded rat brain using DKC1 Rabbit mAb (NBP3-16405) at dilution of 1:100 (40x lens).Perform microwave antigen ...read more
Immunohistochemistry-Paraffin: DKC1 Antibody (2W2V6) [NBP3-16405] - Immunohistochemistry of paraffin-embedded human colon using DKC1 Rabbit mAb (NBP3-16405) at dilution of 1:100 (40x lens).Perform microwave antigen ...read more
A synthetic peptide corresponding to a sequence within amino acids 300-400 of human DKC1 (O60832). VMKDSAVNAICYGAKIMLPGVLRYEDGIEVNQEIVVITTKGEAICMAIALMTTAVISTCDHGIVAKIKRVIMERDTYPRKWGLGPKASQKKLMIKQGLLDK
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Gene
DKC1
Purity
Affinity purified
Innovator's Reward
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58 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Publications
Read Publication using NBP3-16405 in the following applications:
DKC1 is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the NOLA1, 2 and 3 proteins. The protein encoded by this gene and the three NOLA proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. These four H/ACA snoRNP proteins are also components of the telomerase complex. The protein encoded by this gene is related to the Saccharomyces cerevisiae Cbf5p and Drosophila melanogaster Nop60B proteins. The gene lies in a tail-to-tail orientation with the palmitoylated erythrocyte membrane protein gene and is transcribed in a telomere to centromere direction. Both nucleotide substitutions and single trinucleotide repeat polymorphisms have been found in this gene. Mutations in this gene cause X-linked dyskeratosis congenita, a disease resulting in reticulate skin pigmentation, mucosal leukoplakia, nail dystrophy, and progressive bone marrow failure in most cases. Mutations in this gene also cause Hoyeraal-Hreidarsson syndrome, which is a more severe form of dyskeratosis congenita. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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