Apobec1 Antibody (N-term) 精选
Purified Rabbit Polyclonal Antibody (Pab)
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Application
| IHC-P, WB, E |
|---|---|
| Primary Accession | P41238 |
| Other Accession | NP_001635 |
| Reactivity | Human |
| Predicted | Mouse, Rat, Rabbit |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 28192 Da |
| Antigen Region | 7-36 aa |
| Gene ID | 339 |
|---|---|
| Other Names | C->U-editing enzyme APOBEC-1, 354-, Apolipoprotein B mRNA-editing enzyme 1, HEPR, APOBEC1 |
| Target/Specificity | This Apobec1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 7-36 amino acids from the N-terminal region of human Apobec1. |
| Dilution | IHC-P~~1:100~500 WB~~1:1000 E~~Use at an assay dependent concentration. |
| 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 | Apobec1 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
For Research Use Only. Not For Use In Diagnostic Procedures.
| Name | APOBEC1 (HGNC:604) |
|---|---|
| Function | Cytidine deaminase catalyzing the cytidine to uridine postranscriptional editing of a variety of mRNAs (PubMed:30844405). Form complexes with cofactors that confer differential editing activity and selectivity. Responsible for the postranscriptional editing of a CAA codon for Gln to a UAA codon for stop in the apolipoprotein B mRNA (PubMed:24916387). Also involved in CGA (Arg) to UGA (Stop) editing in the NF1 mRNA (PubMed:11727199). May also play a role in the epigenetic regulation of gene expression by participating in DNA demethylation (By similarity). |
| Cellular Location | Cytoplasm. Nucleus |
| Tissue Location | Expressed exclusively in the small intestine. |
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
APOBEC1 is involved in the production of apolipoprotein B (apoB)-48 from apoB-100. The gene spans 18 kb and contains five exons, all of which are translated. Alternative splicing produces a variant transcript that lacks exon 2 and encodes a novel 36-amino acid peptide. The exon 2-skipped transcript accounts for approximately 50% of APOBEC1 mRNA in the adult small intestine and up to 90% of APOBEC1 mRNA in the developing gut. Exon 2-skipping may thus be a quantitatively important mechanism for regulating the expression of this gene in the gastrointestinal tract.
REFERENCES
Blanc, V., et al., J. Biol. Chem. 278(42):41198-41204 (2003).
Chester, A., et al., EMBO J. 22(15):3971-3982 (2003).
Wedekind, J.E., et al., Trends Genet. 19(4):207-216 (2003).
Mukhopadhyay, D., et al., Am. J. Hum. Genet. 70(1):38-50 (2002).
Dance, G.S., et al., J. Biol. Chem. 277(15):12703-12709 (2002).
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