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Anti-Corticotropin Releasing Factor Receptor 2 antibody
See all Corticotropin Releasing Factor Receptor 2 products (2) ...
Rabbit polyclonal to Corticotropin Releasing Factor Receptor 2
ab75168 detects endogenous levels of total CRFR2 protein
WB, ELISA, IHC-Pmore details
Reacts with
Mouse, Rat, Human
synthetic peptide derived from internal region of human Corticotropin Releasing Factor Receptor 2
extracts from K562 cells, LOVO cells, 3T3 cells and RAW264.7 cells
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS (without Mg2+ and Ca2+), 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Neuroscience >> Endocrine system >> Hypothalamic pituitary adrenal axis
Neuroscience >> Neurotransmission >> Receptors / Channels >> GPCR >> More GPCR
Our Abpromise guarantee covers the use of ab75168 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/500 - 1/1000.Predicted molecular weight: 48 kDa.
ELISA: 1/10000
IHC-P: Use a concentration of 1 µg/mlPerform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
This is a receptor for corticotropin releasing factor. Shows high-affinity CRF binding. Also binds to urocortin I, II and III. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase.
Belongs to the G-protein coupled receptor 2 family.
Cell membrane.
Target information above from: UniProt accessionQ13324
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Corticotropin Releasing Factor Receptor 2 antibody (ab75168)
All lanes : Anti-Corticotropin Releasing Factor Receptor 2 antibody (ab75168) at 1/500 dilution
Lane 1 : extracts from K562 cells
Lane 2 : extracts from LOVO
cells
Lane 3 : extracts from 3T3 cells
Lane 4 : extracts from RAW264.7 cells
Lane 5 : extracts from 3T3 cells with immunising peptide at 10ug
Lysates/proteins at 30 µg per lane.
Predicted band size : 48 kDa
Observed band size : 48 kDa
Additional bands at : 80 kDa. We are unsure as to the identity of these extra bands.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)-Corticotropin Releasing Factor Receptor 2 antibody(ab75168)

IHC image of ab75168 staining in human normal skeletal muscle formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH9, epitope retrieval solution 2) for 20 mins. The section was then incubated with ab75168, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
ab75168 has not yet been referenced specifically in any publications.
Publishing research using ab75168? Please let us know so that we can cite the reference in this datasheet
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All lanes : Anti-Corticotropin Releasing Factor Receptor 2 antibody (ab75168) at 1/500 dilution
Lane 1 : extracts from K562 cells
Lane 2 : extracts from LOVO
cells
Lane 3 : extracts from 3T3 cells
Lane 4 : extracts from RAW264.7 cells
Lane 5 : extracts from 3T3 cells with immunising peptide at 10ug
Lysates/proteins at 30 µg per lane.
Predicted band size : 48 kDa
Observed band size : 48 kDa
Additional bands at : 80 kDa. We are unsure as to the identity of these extra bands.

IHC image of ab75168 staining in human normal skeletal muscle formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH9, epitope retrieval solution 2) for 20 mins. The section was then incubated with ab75168, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
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