Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Western blot [1]
- Other assay [1]
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Validation data
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- Product number
- PA5-96439 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- Prodynorphin Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Recombinant full-length protein
- Description
- Immunogen sequence: DCLSRCSLCA VKTQDGPKPI NPLICSLQCQ AALLPSEEWE RCQSFLSFFT PSTLGLNDKE DLGSKSVGEG PYSELAKLSG SFLKELEKSK FLPSISTKEN TLSKSLEEKL RGLSDGFREG AESELMRDAQ LNDGAMETGT LYLAEEDPKE QVKRYGGFLR KYPKRSSEVA GEGDGDSMGH EDLYKRYGGF LRRIRPKLKW DNQKRYGGFL RRQFKVVTRS QEDPNAYSGE LFDA; Positive Samples: U-251MG, Mouse liver, Mouse pancreas
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 0.92 mg/mL
- Storage
- -20° C, Avoid Freeze/Thaw Cycles
Submitted references Adjusting vascular permeability, leukocyte infiltration, and microglial cell activation to rescue dopaminergic neurons in rodent models of Parkinson's disease.
Optogenetic activation of striatal D1R and D2R cells differentially engages downstream connected areas beyond the basal ganglia.
Cai HY, Fu XX, Jiang H, Han S
NPJ Parkinson's disease 2021 Oct 8;7(1):91
NPJ Parkinson's disease 2021 Oct 8;7(1):91
Optogenetic activation of striatal D1R and D2R cells differentially engages downstream connected areas beyond the basal ganglia.
Grimm C, Frässle S, Steger C, von Ziegler L, Sturman O, Shemesh N, Peleg-Raibstein D, Burdakov D, Bohacek J, Stephan KE, Razansky D, Wenderoth N, Zerbi V
Cell reports 2021 Dec 28;37(13):110161
Cell reports 2021 Dec 28;37(13):110161
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western Blot analysis of Prodynorphin in extracts of various cell lines using Prodynorphin Polyclonal Antibody (Product # PA5-96439) at a dilution of 1:1000. A HRP Goat Anti-Rabbit IgG (H+L) secondary antibody was used at a dilution of 1:10,000. Lysates/proteins: 25 µg per lane. Blocking buffer: 3% nonfat dry milk in TBST.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Fig. 15 C16 in combination with Ang-1 treatment decreased the expression of phospho-DARPP-32, and increased the expression of pdyn and PPE. Western blot analysis showed no significant difference in the expression of DARPP-32 among the different groups ( a , b ). The expression of phospho-DARPP-32 in the vehicle-treated group was higher than that in normal controls ( c , d ). The combination of C16 and Ang-1 inhibited the upregulation of phospho-DARPP-32 in model animals. The downregulation of prodynorphin (pdyn, e , f ) and the upregulation of preproenkephalin (PPE, g , h ) in the model groups were remarkably reversed by treatment with C16, Ang-1, and C16 plus Ang-1. a p < 0.05 versus the normal control group; b p < 0.05 versus the vehicle group ( c ), p < 0.05 versus the C16-treated group ( d ), p < 0.05 versus the Ang-1-treated group. Darpp-32 protein: 34 kDa; pDarpp-32 protein: 34 kDa; Pdyn protein: 28 kDa; PPE protein: 30 kDa; beta-actin protein: 42 kDa; Abbreviations: DARPP, dopamine- and cAMP-regulated neuronal phosphoprotein; pdyn, prodynorphin; PPE, preproenkephalin; C16, peptide (KAFDITYVRLKF) that can selectively bind integrin alpha nu beta 3 ; Ang-1, angiopoietin-1.