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Anti-Human APOBEC3H Polyclonal Antibody (HB477014)

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Overview
Catalog No.HB477014
Description
Anti-Human APOBEC3H Polyclonal Antibody (HB477014) is a rabbit polyclonal antibody detecting DNA dC->dU-editing enzyme APOBEC-3H; 3.5.4.38; APOBEC-related protein 10; ARP-10; Apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3H; A3H; APOBEC3H in ELISA, IHC, WB. Suitable for Human.
Highlights
  • Affinity Purified — Minimal background and high purity for reliable results.
  • Multi-Application — Validated across multiple applications.
Species reactivityHuman
ApplicationsELISA, IHC, WB
Host speciesRabbit
IsotypeIgG
Clonality Polyclonal
Immunogen E. coli - derived recombinant human APOBEC3H (Met1-Val200).
Target DNA dC->dU-editing enzyme APOBEC-3H; 3.5.4.38; APOBEC-related protein 10; ARP-10; Apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3H; A3H; APOBEC3H
Endotoxin level Please contact with the lab for this information.
Purification Purified by antigen affinity column.
Accession Q6NTF7
Form Liquid
Storage buffer 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Product Usage Information
Application Dilution
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Background

DNA dC->dU-editing enzyme APOBEC-3H (APOBEC3H) is a ~23 kDa protein. DNA deaminase (cytidine deaminase) which acts as an inhibitor of retrovirus replication and retrotransposon mobility via deaminase-dependent and -independent mechanisms. The A3H-var/haplotype 2 exhibits antiviral activity against vif-deficient HIV-1. After the penetration of retroviral nucleocapsids into target cells of infection and the initiation of reverse transcription, it can induce the conversion of cytosine to uracil in the minus-sense single-strand viral DNA, leading to G-to-A hypermutations in the subsequent plus-strand viral DNA. The resultant detrimental levels of mutations in the proviral genome, along with a deamination-independent mechanism that works prior to the proviral integration, together exert efficient antiretroviral effects in infected target cells. Selectively targets single-stranded DNA and does not deaminate double-stranded DNA or single- or double-stranded RNA.

1. OhAinle, M. et al. (2006) Journal of virology 80, 3853-62. PMID: 16571802
2. Dang, Y. et al. (2006) Journal of virology 80, 10522-33. PMID: 16920826
3. OhAinle, M. et al. (2008) Cell host & microbe 4, 249-59. PMID: 18779051
4. Tan, L. et al. (2009) FASEB journal : official publication of the Federation of American Societies for Experimental Biology 23, 279-87. PMID: 18827027
5. Stenglein, MD. et al. (2010) Nature structural & molecular biology 17, 222-9. PMID: 20062055
6. Phalora, PK. et al. (2012) Journal of virology 86, 11712-24. PMID: 22915799
7. Shaban, NM. et al. (2018) Molecular cell 69, 75-86.e9. PMID: 29290613
8. Dang, Y. et al. (2008) The Journal of biological chemistry 283, 11606-14. PMID: 18299330
9. Hultquist, JF. et al. (2011) Journal of virology 85, 11220-34. PMID: 21835787
10. Chaipan, C. et al. (2013) Journal of virology 87, 444-53. PMID: 23097438
Note For research use only
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Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
Enter any 2 of Mass, Concentration, Volume + Molecular Weight to solve for the unknown.
Mass
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Volume
Molecular Weight *
g/mol
Formula
C₁ × V₁ = C₂ × V₂
Enter any 3 of the 4 values to solve for the unknown.
Stock Solution
C₁ (Stock Conc.)
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V₁ (Stock Vol.)
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Working Solution
C₂ (Working Conc.)
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