AP3184a
antibody from Abgent
Targeting: CDKN2A
ARF, CDK4I, CDKN2, CMM2, INK4, INK4a, MLM, MTS1, p14, p14ARF, p16, p16INK4a, p19, p19Arf
Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Western blot [1]
- Immunohistochemistry [1]
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Validation data
Reference
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- Product number
- AP3184a - Provider product page
- Provider
- Abgent
- Proper citation
- Abgent Cat#AP3184a, RRID:AB_2078287
- Product name
- Phospho-p16-INK4A(S152) Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Description
- Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 400 µl
- Storage
- Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Submitted references The atr protein kinase controls UV-dependent upregulation of p16INK4A through inhibition of Skp2-related polyubiquitination/degradation.
Overexpression of the transcription factor Yin-Yang-1 suppresses differentiation of HaCaT cells in three-dimensional cell culture.
Al-Khalaf HH, Hendrayani SF, Aboussekhra A
Molecular cancer research : MCR 2011 Mar;9(3):311-9
Molecular cancer research : MCR 2011 Mar;9(3):311-9
Overexpression of the transcription factor Yin-Yang-1 suppresses differentiation of HaCaT cells in three-dimensional cell culture.
Taguchi S, Kawachi Y, Ishitsuka Y, Fujisawa Y, Furuta J, Nakamura Y, Xu X, Ikebe D, Kato M, Otsuka F
The Journal of investigative dermatology 2011 Jan;131(1):37-45
The Journal of investigative dermatology 2011 Jan;131(1):37-45
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Supportive validation
- Submitted by
- Abgent (provider)
- Main image
- Experimental details
- The anti-Phospho-p16-INK4A-S152 Pab (Cat. #AP3184a) is used in Western blot to detect Phospho-p16-INK4A-S152 in A2058 tissue lysate
- Primary Ab dilution
- 1:1000
Supportive validation
- Submitted by
- Abgent (provider)
- Main image
- Experimental details
- "Formalin-fixed and paraffin-embedded human cancer tissue reacted with the primary antibody, which was peroxidase-conjugated to the secondary antibody, followed by AEC staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated. BC = breast carcinoma; HC = hepatocarcinoma."
- Primary Ab dilution
- 1:50~100