NMD3 Antibody (C-term)
Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, E |
---|---|
Primary Accession | Q96D46 |
Reactivity | Human, Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 57603 Da |
Antigen Region | 410-440 aa |
Gene ID | 51068 |
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Other Names | 60S ribosomal export protein NMD3, hNMD3, NMD3 |
Target/Specificity | This NMD3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 410-440 amino acids from the C-terminal region of human NMD3. |
Dilution | WB~~1:1000 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | NMD3 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | NMD3 |
---|---|
Function | Acts as an adapter for the XPO1/CRM1-mediated export of the 60S ribosomal subunit. |
Cellular Location | Cytoplasm. Nucleus. Note=Shuttles between the nucleus/nucleolus and the cytoplasm in a XPO1/CRM1-dependent manner |
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Provided below are standard protocols that you may find useful for product applications.
Background
It has been suggested that NMD3 is a cytoplasmic factor required for a late cytoplasmic assembly step of the 60S subunit but is not a ribosomal protein. A mutation in NMD3 was found to be lethal in the absence of XRN1, which encodes the major cytoplasmic exoribonuclease responsible for mRNA turnover. The NMD3 protein sequence does not contain readily recognizable motifs of known function. However, NMD3 orthologues display an amino-terminal domain containing four repeats of Cx2C, reminiscent of zinc-binding proteins, implicated in nucleic acid binding or protein oligomerization.
References
Trotta, C.R., et al., EMBO J. 22(11):2841-2851 (2003).
Ho, J.H. et al., Mol. Cell. Bio., 19(3):2389-2399 (1999).
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