Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Western blot [1]
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Validation data
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- Product number
- MAB1927 - Provider product page
- Provider
- Novus Biologicals
- Product name
- Rat Monoclonal BMP-1/PCP Antibody
- Antibody type
- Monoclonal
- Description
- Protein A or G purified from hybridoma culture supernatant. Detects human BMP-1/PCP in direct ELISAs and Western blots.
- Reactivity
- Human
- Host
- Rat
- Isotype
- IgG
- Vial size
- 500 ug
- Concentration
- LYOPH
- Storage
- Use a manual defrost freezer and avoid repeated freeze-thaw cycles. 12 months from date of receipt, -20 to -70 degreesC as supplied. 1 month, 2 to 8 degreesC under sterile conditions after reconstitution. 6 months, -20 to -70 degreesC under sterile conditions after reconstitution.
Submitted references Bone morphogenetic protein 1 is expressed in porcine ovarian follicles and promotes oocyte maturation and early embryonic development.
Identification of a potential cardiac antifibrotic mechanism of torasemide in patients with chronic heart failure.
Lei X, Cui K, Cai X, Ren Y, Liu Q, Shi D
The Journal of veterinary medical science 2017 Feb 4;79(2):258-266
The Journal of veterinary medical science 2017 Feb 4;79(2):258-266
Identification of a potential cardiac antifibrotic mechanism of torasemide in patients with chronic heart failure.
López B, González A, Beaumont J, Querejeta R, Larman M, Díez J
Journal of the American College of Cardiology 2007 Aug 28;50(9):859-67
Journal of the American College of Cardiology 2007 Aug 28;50(9):859-67
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Supportive validation
- Submitted by
- Novus Biologicals (provider)
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- Experimental details
- Detection of Human BMP-1/PCP by Western Blot. Western blot shows lysates of Jurkat human acute T cell leukemia cell line and human skin tissue. PVDF Membrane was probed with 2 µg/mL of Human BMP-1/PCP Monoclonal Antibody (Catalog # MAB1927) followed by HRP-conjugated Anti-Rat IgG Secondary Antibody (Catalog # HAF005). A specific band was detected for BMP-1/PCP at approximately 180 kDa (as indicated). This experiment was conducted under non-reducing conditions and using Immunoblot Buffer Group 1.