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Western blotAntibody data
- Antibody Data
- Antigen structure
- References [1]
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- Validations
- Western blot [3]
- Other assay [1]
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- Product number
- PA5-44912 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- AZGP1 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- Peptide sequence: MVRMVPVLLS LLLLLGPAV P QENQDGRY SL TYIYTGL SKH VEDVPA FQAL Sequence homology: Dog: 79%; Human: 100%
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 0.5 mg/mL
- Storage
- -20° C, Avoid Freeze/Thaw Cycles
Submitted references RNA-Seq Analysis of Differentiated Keratinocytes Reveals a Massive Response to Late Events during Human Papillomavirus 16 Infection, Including Loss of Epithelial Barrier Function.
Klymenko T, Gu Q, Herbert I, Stevenson A, Iliev V, Watkins G, Pollock C, Bhatia R, Cuschieri K, Herzyk P, Gatherer D, Graham SV
Journal of virology 2017 Dec 15;91(24)
Journal of virology 2017 Dec 15;91(24)
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of human 293T cells using an anti-AZGP1 polyclonal antibody (Product # PA5-44912).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of human 293T cells using an anti-AZGP1 polyclonal antibody (Product # PA5-44912).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of human heart cells using an anti-AZGP1 polyclonal antibody (Product # PA5-44912).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- FIG 6 Western blot analysis of protein levels encoded by selected, significantly altered mRNAs ( Table 2 ). Protein extracts were prepared from undifferentiated (U) and differentiated (D) HPV-negative NIKS and HPV16-positive NIKS16 and W12 cell populations. Much greater levels of involucrin (invol) were detected in the differentiated than in the undifferentiated cell populations, indicating that differentiation was achieved. GAPDH was used as a protein loading control. (A) Protein levels corresponding to significantly upregulated mRNAs; (B) protein levels corresponding to significantly downregulated mRNAs.
