Antibody data
- Antibody Data
- Antigen structure
- References [0]
- Comments [0]
- Validations
- Immunocytochemistry [2]
- Chromatin Immunoprecipitation [2]
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Validation data
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- Product number
- 703052 - Provider product page

- Provider
- Invitrogen Antibodies
- Product name
- C17orf96 Recombinant Rabbit Monoclonal Antibody (5H7L8)
- Antibody type
- Monoclonal
- Antigen
- Synthetic peptide
- Description
- This antibody is predicted to react with Monkey, Pig, Cat, Dog. Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. The expression systems are developed by cloning in the specific antibody DNA sequences from immunoreactive rabbits. Then, individual clones are screened to select the best candidates for production. The advantages of using recombinant rabbit monoclonal antibodies include: better specificity and sensitivity, lot-to-lot consistency, animal origin-free formulations, and broader immunoreactivity to diverse targets due to larger rabbit immune repertoire.
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Isotype
- IgG
- Antibody clone number
- 5H7L8
- Vial size
- 100 μg
- Concentration
- 0.5 mg/mL
- Storage
- Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image

- Experimental details
- For immunofluorescence analysis, HEK-293 cells were fixed and permeabilized for detection of endogenous C17orf96 using Anti-C17orf96 Recombinant Rabbit Monoclonal Antibody (Product # 703052, 1:100 dilution) and labeled with Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate (Product # A27034, 1:2000). Panel a) shows representative cells that were stained for detection and localization of C17orf96 protein (green), Panel b) is stained for nuclei (blue) using ProLong™ Diamond Antifade Mountant with DAPI (Product # P36962). Panel c) represents cytoskeletal F-actin staining using Rhodamine Phalloidin (Product # R415, 1:300). Panel d) is a composite image of Panels a, b and c clearly demonstrating nuclear localization of C17orf96. Panel e) represents control cells with no primary antibody to assess background. The images were captured at 60X magnification.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image

- Experimental details
- For immunofluorescence analysis, HEK-293 cells were fixed and permeabilized for detection of endogenous C17orf96 using Anti-C17orf96 Recombinant Rabbit Monoclonal Antibody (Product # 703052, 1:100 dilution) and labeled with Goat anti-Rabbit IgG (Heavy Chain) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate (Product # A27034, 1:2000). Panel a) shows representative cells that were stained for detection and localization of C17orf96 protein (green), Panel b) is stained for nuclei (blue) using ProLong™ Diamond Antifade Mountant with DAPI (Product # P36962). Panel c) represents cytoskeletal F-actin staining using Rhodamine Phalloidin (Product # R415, 1:300). Panel d) is a composite image of Panels a, b and c clearly demonstrating nuclear localization of C17orf96. Panel e) represents control cells with no primary antibody to assess background. The images were captured at 60X magnification.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image

- Experimental details
- Enrichment of endogenous C17ORF96 protein at specific gene loci using Anti-C17ORF96 Antibody: Chromatin Immunoprecipitation (ChIP) was performed using Anti-C17ORF96 Recombinant Rabbit Monoclonal Antibody (Product # 703052, 5 µg) on sheared chromatin from 2 million HEK-293 cells using the MAGnify ChIP System kit (Product # 492024). Normal Rabbit IgG was used as a negative IP control. The purified DNA was analyzed by qPCR with PCR primer pairs over Promoters of HOXA9, MYT1, SOX2 and SAT2 satellite repeats . Data is presented as fold enrichment of the antibody signal versus the negative control IgG using the comparative CT method.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image

- Experimental details
- Enrichment of endogenous C17ORF96 protein at specific gene loci using Anti-C17ORF96 Antibody: Chromatin Immunoprecipitation (ChIP) was performed using Anti-C17ORF96 Recombinant Rabbit Monoclonal Antibody (Product # 703052, 5 µg) on sheared chromatin from 2 million HEK-293 cells using the MAGnify ChIP System kit (Product # 492024). Normal Rabbit IgG was used as a negative IP control. The purified DNA was analyzed by qPCR with PCR primer pairs over Promoters of HOXA9, MYT1, SOX2 and SAT2 satellite repeats . Data is presented as fold enrichment of the antibody signal versus the negative control IgG using the comparative CT method.