Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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- Product number
- M00273-3 - Provider product page
- Provider
- Boster Biological Technology
- Product name
- Anti-PAX6 Rabbit Monoclonal Antibody
- Antibody type
- Monoclonal
- Description
- Monoclonal antibody for PAX 6/PAX6 detection. Host: Rabbit.Size: 100ug/vial. Tested applications: IF, IHC, ICC, WB. Reactive species: Human, Mouse, Rat PAX 6/PAX6 information: Molecular Weight: 46683 MW; Subcellular Localization: Nucleus; Tissue Specificity: Fetal eye, brain, spinal cord and olfactory epithelium. Isoform 5a is less abundant than the PAX6 shorter form.
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Antibody clone number
- HGF-16
- Vial size
- 100ug/vial
- Concentration
- 0.5-1mg/ml, actual concentration vary by lot. Use suggested dilution ratio to decide dilution procedure.
- Storage
- At -20°C for one year. Avoid repeated freezing and thawing.
Submitted references Japanese medaka Olpax6.1 mutant as a potential model for spondylo-ocular syndrome.
Medaka (Oryzias latipes) Olpax6.2 acquires maternal inheritance and germ cells expression, but functionally degenerate in the eye.
Microvesicles Derived from Human Embryonic Neural Stem Cells Inhibit the Apoptosis of HL-1 Cardiomyocytes by Promoting Autophagy and Regulating AKT and mTOR via Transporting HSP-70.
Pan Q, Lu K, Luo J, Jiang Y, Xia B, Chen L, Wang M, Dai R, Chen T
Functional & integrative genomics 2023 May 19;23(2):168
Functional & integrative genomics 2023 May 19;23(2):168
Medaka (Oryzias latipes) Olpax6.2 acquires maternal inheritance and germ cells expression, but functionally degenerate in the eye.
Pan Q, Luo J, Jiang Y, Wang Z, Lu K, Chen T
Gene 2023 Jul 1;872:147439
Gene 2023 Jul 1;872:147439
Microvesicles Derived from Human Embryonic Neural Stem Cells Inhibit the Apoptosis of HL-1 Cardiomyocytes by Promoting Autophagy and Regulating AKT and mTOR via Transporting HSP-70.
Zhang L, Gao J, Chen T, Chen X, Ji X, Ye K, Yu J, Tang B, Wei Y, Xu H, Hu J
Stem cells international 2019;2019:6452684
Stem cells international 2019;2019:6452684
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