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POLR1D antibody
POLR1D
Reactivity: Human
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-POLR1D Antibody
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Target
See all POLR1D Antibodies
POLR1D
(Polymerase (RNA) I Polypeptide D, 16kDa (POLR1D))
Reactivity
All reactivities for POLR1D antibodies
Human
Host
All hosts for POLR1D antibodies
Rabbit
Clonality
All clonalities for POLR1D antibodies
Polyclonal
Conjugate
All conjugates for POLR1D antibodies
This POLR1D antibody is un-conjugated
Application
All applications for POLR1D antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Antigen affinity purification
Immunogen
Fusion protein of human POLR1D
Isotype
IgG
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Discover our top product POLR1D Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:300, ELISA 1:5000-1:10000
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.84 mg/mL
Buffer
PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for POLR1D
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Target
POLR1D
(Polymerase (RNA) I Polypeptide D, 16kDa (POLR1D))
Alternative Name
POLR1D (POLR1D Products )
Synonyms
AC19 antibody, POLR1C antibody, RPA16 antibody, RPA9 antibody, RPAC2 antibody, RPC16 antibody, RPO1-3 antibody, TCS2 antibody, 1110003G10Rik antibody, Rpo1-3 antibody, im:7162148 antibody, zgc:136449 antibody, polr1d antibody, rpa16 antibody, rpa9 antibody, rpac2 antibody, rpo1-3 antibody, RNA polymerase I subunit D antibody, polymerase (RNA) I polypeptide D antibody, polymerase (RNA) I polypeptide D, 16kDa, gene 2 L homeolog antibody, POLR1D antibody, Polr1d antibody, polr1d antibody, polr1d.2.L antibody
Background
The protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants.
UniProt
Q9Y2S0
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