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Rabbit Anti-POLR1D Antibody (CSB-PA897095ESR1HU)
Supplier: CUSABIO BIOTECH CO.
RNA polymerases I and III subunit AC2 Antibody,AC19 Antibody,DNA-directed RNA polymerase I subunit D Antibody,RNA polymerase I 16 kDa subunit Antibody, RPA16 Antibody,RPC16 Antibody,hRPA19 Antibody,POLR1D AntibodyMore alternative names for the antibody
AC19 antibody|DNA directed RNA polymerase I 16 kDa polypeptide antibody|DNA directed RNA polymerase I subunit D antibody|DNA directed RNA polymerases I and III subunit RPAC2 antibody|DNA-directed RNA polymerase I subunit D antibody|DNA-directed RNA polymerases I and III subunit RPAC2 antibody|FLJ20616 antibody|hRPA19 antibody|MGC9850 antibody|POLR1C antibody|POLR1D antibody|Polymerase (RNA) I polypeptide D antibody|Polymerase (RNA) I polypeptide D, 16kDa antibody|RNA polymerase I 16 kDa subunit antibody|RNA polymerases I and III subunit AC2 antibody|RPA16 antibody|RPA9 antibody|RPAC2 antibody|RPAC2_HUMAN antibody|RPC16 antibody|RPO1 3 antibody
Anti-POLR1D antibody (ab104115)
Anti-POLR1D antibody (ab104115)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human DNA-directed RNA polymerases I and III subunit RPAC2 protein (1-133AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:539061( Cow), Entrez Gene:51082( Human), Entrez Gene:20018( Mouse), Omim:613715( Human), SwissProt:Q1RMG8( Cow), SwissProt:Q9Y2S0( Human), SwissProt:P97304( Mouse), Unigene:507584( Human), Unigene:735744( Human), Unigene:317557( Mouse)
|Protein function|| |
DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. Common core component of RNA polymerases I and III which synthesize ribosomal RNA precursors and small RNAs, such as 5S rRNA and tRNAs, respectively.
|Involvement in disease|| |
Treacher Collins syndrome 2 (TCS2) [MIM:613717]: A form of Treacher Collins syndrome, a disorder of craniofacial development. Treacher Collins syndrome is characterized by a combination of bilateral downward slanting of the palpebral fissures, colobomas of the lower eyelids with a paucity of eyelashes medial to the defect, hypoplasia of the facial bones, cleft palate, malformation of the external ears, atresia of the external auditory canals, and bilateral conductive hearing loss. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the archaeal RpoL/eukaryotic RPB11/RPC19 RNA polymerase subunit family.
|Protein cellular localization|| |
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|Product type|| |
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