Antibody data
- Antibody Data
- Antigen structure
- References [0]
- Comments [0]
- Validations
- Western blot [2]
- Immunocytochemistry [2]
- Immunohistochemistry [2]
- Other assay [2]
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- Product number
- PA5-104508 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- Collagen IV Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- Antibody detects endogenous levels of total Collagen IV.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 1 mg/mL
- Storage
- -20°C
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Supportive validation
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- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of Collagen IV in 293 and HeLa (Lane 1: 293 cells, Lane 2: Hela cells, Lane 3: 293 cells treated with blocking peptide). Samples were incubated with Collagen IV polyclonal antibody (Product # PA5-104508).
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- Invitrogen Antibodies (provider)
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- Experimental details
- Western blot analysis of Collagen IV in 293 and HeLa (Lane 1: 293 cells, Lane 2: Hela cells, Lane 3: 293 cells treated with blocking peptide). Samples were incubated with Collagen IV polyclonal antibody (Product # PA5-104508).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescent analysis of Collagen IV in HeLa cells. Samples were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100, blocked with 10% serum (45 min at 25°C) incubated with Collagen IV polyclonal antibody (Product # PA5-104508) using a dilution of 1:200 (1 hr, 37°C), and followed by goat anti-rabbit IgG Alexa Fluor 594 at a dilution of 1:600.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunofluorescent analysis of Collagen IV in HeLa cells. Samples were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100, blocked with 10% serum (45 min at 25°C) incubated with Collagen IV polyclonal antibody (Product # PA5-104508) using a dilution of 1:200 (1 hr, 37°C), and followed by goat anti-rabbit IgG Alexa Fluor 594 at a dilution of 1:600.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
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- Experimental details
- Immunohistochemistry analysis of paraffin-embedded Collagen IV in human colon cancer tissues sections. Antigen retrieval was performed using citrate buffer. Samples were blocked with blocking buffer (1.5 hr, 22°C), incubated with Collagen IV polyclonal antibody (Product # PA5-104508) using a dilution of 1:100 (1.5 hr, 22°C), followed by HRP conjugated goat anti-rabbit.
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- Invitrogen Antibodies (provider)
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- Experimental details
- Immunohistochemistry analysis of paraffin-embedded Collagen IV in human Melanoma tissue. Antigen retrieval was performed using citrate buffer. Samples were blocked with blocking buffer (1.5 hr, 22°C), incubated with Collagen IV polyclonal antibody (Product # PA5-104508) using a dilution of 1:100 (1.5 hr, 22°C), followed by HRP conjugated goat anti-rabbit.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- FIGURE 2 TIMP3 overexpression in macrophages reduces STZ-induced inflammation and fibrosis in kidney. Kidney cortex analysis of (A) gene expression of F4/80, MCP1, TNF-alpha, IL6, and COL1A2 and (B) protein levels of WT1, Podocin, Nephrin, Coll-IV, TGF-beta, Actin, phospho-p38 (p-p38), p38 in wt, and MacT3 non-diabetic and diabetic mice (n = 6 per group). (C) Protein levels of WT1, Podocin, and Actin in kidney glomerular fraction of wt and MacT3 non-diabetic and diabetic mice (n = 5 per group). A representative image of two mice per group is shown. Relative protein levels as determined by densitometry (*p < 0.05, **p
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- Invitrogen Antibodies (provider)
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- Experimental details
- FIGURE 4 Podocyte deletion of ADAM17 attenuates STZ-induced injury in kidney. Twelve weeks after STZ administration diabetic Ct and DeltaPodA17 mice and age-matched non-diabetic littermates (Ctrl) were analyzed for (A) PAS-staining in kidney and quantification of mGA, fMA, and mMA (arrows indicate glomerular hypertrophy and mesangial expansion) and (B) immunohistochemical staining of Nox4 and Coll-IV in kidney (non-diabetic n = 5, diabetic n = 10 per group, original magnification, X400) (arrows indicate increased glomerular staining for Nox4 and Coll-IV). (C) Protein expression of WT1, Podocin, Nephrin, Coll-IV, and Actin in kidney cortex from Ct and DeltaPodA17 non-diabetic and diabetic mice (n = 6 per group). A representative image of two mice per group is shown. Relative protein levels as determined by densitometry (*p < 0.05, **p