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GR32L Anti-Glucocorticoid Receptor (Ab-2) Mouse mAb (BuGR2)

GR32L
Purchase on Sigma-Aldrich

Přehled

Replacement Information

Tabulka spec. kláve

Species ReactivityHostAntibody Type
Gp, M, Rb, R, ShMMonoclonal Antibody

Products

Katalogové čísloBalení ks/bal.
GR32L-100UG Plastová ampulka 100 μg
Description
OverviewRecognizes the ~94-97 kDa glucocorticoid receptor in mouse liver tissue.
Catalogue NumberGR32L
Brand Family Calbiochem®
Application Data
Detection of mouse glucocorticoid receptor by immunoblotting. Sample: Whole tissue extract from mouse liver. Primary antibody: Anti-Glucocorticoid Receptor (Ab-2) Mouse mAb (BuGR2) (Cat No. GR32L) (5 µg/ml). Detection: chemiluminescence.
References
ReferencesHussien, A., et al. 1997. Proc. Natl. Acad. Sci. USA 94, 1521.
Pratt, W.B. and Toft, D.O., 1997. Endocrine Rev. 18 306.
Schumacher, M., et al. 1996. Dev. Neurosci. 18, 6.
Toran-Allerand, C.D. 1996. Dev. Neurosci. 18, 36.
Weigel, N.L. 1996. Biochem J. 319, 657.
Jones, K.J. 1994. Ann. N.Y. Acad. Sci. 743, 141.
Arnold, A.P. 1990. in Hormones, Brain and Behavior in Vertebrates, ed. Balthazart, J. (Karger, Basel), 82.
Product Information
FormLyophilized
FormulationLyophilized from PBS, pH 7.2.
Positive controlmouse liver extract
Preservative≤0.1% sodium azide
Quality LevelMQ100
Applications
Application ReferencesOriginal Clone Gametchu, B. and Harrison, R., 1984. Endocrinology 114, 274.
Key Applications Frozen Sections
Immunoblotting (Western Blotting)
Immunocytochemistry
Immunoprecipitation
Paraffin Sections
Application NotesFrozen Sections (5 µg/ml)
Immunoblotting (5 µg/ml)
Immunocytochemistry (5 µg/ml)
Immunoprecipitation (see comments)
Paraffin Sections (5 µg/ml)
Application CommentsDoes not cross react with androgen, progesterone, estrogen or mineralocorticoid receptors. Enzymatic digestion and immunoblot analysis has shown that this antibody reacts with the undigested 97 kDa glucocorticoid receptor, a 17 kDa DNA-binding trypsin fragment, and a 45 kDa steroid and DNA-binding chymotrypsin fragment. Immunocytochemical localization of the glucocorticoid receptor is observed in the cytoplasm and nucleus, even in the presence of hormone. This antibody has also been reported to work for immunoprecipitation. Antibody should be titrated for optimal results in individual systems.
Biological Information
Immunogenpartially purified, rat glucocorticoid receptor
ImmunogenRat
CloneBuGR2
HostMouse
IsotypeIgG2a
Species Reactivity
  • Guinea Pig
  • Mouse
  • Rabbit
  • Rat
  • Sheep
Antibody TypeMonoclonal Antibody
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Standard Handling
Storage -20°C
Do not freeze Ok to freeze
Special InstructionsResuspend the lyophilized antibody with 0.1 ml sterile PBS, pH 7.2. Be careful to reconstitute the entire contents of the vial; during shipment and handling, portions of the lyophilized pellet may have become dislodged and may not be in the bottom of the vial. Following reconstitution, aliquot and freeze (-20°C). Avoid freeze/thaw cycles of solutions.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Katalogové číslo GTIN
GR32L-100UG 04055977228298

Documentation

Anti-Glucocorticoid Receptor (Ab-2) Mouse mAb (BuGR2) MSDS

Title

Safety Data Sheet (SDS) 

Anti-Glucocorticoid Receptor (Ab-2) Mouse mAb (BuGR2) Certificates of Analysis

TitleLot Number
GR32L

References

Přehled odkazů
Hussien, A., et al. 1997. Proc. Natl. Acad. Sci. USA 94, 1521.
Pratt, W.B. and Toft, D.O., 1997. Endocrine Rev. 18 306.
Schumacher, M., et al. 1996. Dev. Neurosci. 18, 6.
Toran-Allerand, C.D. 1996. Dev. Neurosci. 18, 36.
Weigel, N.L. 1996. Biochem J. 319, 657.
Jones, K.J. 1994. Ann. N.Y. Acad. Sci. 743, 141.
Arnold, A.P. 1990. in Hormones, Brain and Behavior in Vertebrates, ed. Balthazart, J. (Karger, Basel), 82.
Data Sheet

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision27-August-2007 RFH
ApplicationFrozen Sections (5 µg/ml)
Immunoblotting (5 µg/ml)
Immunocytochemistry (5 µg/ml)
Immunoprecipitation (see comments)
Paraffin Sections (5 µg/ml)
Application Data
Detection of mouse glucocorticoid receptor by immunoblotting. Sample: Whole tissue extract from mouse liver. Primary antibody: Anti-Glucocorticoid Receptor (Ab-2) Mouse mAb (BuGR2) (Cat No. GR32L) (5 µg/ml). Detection: chemiluminescence.
DescriptionPurified mouse monoclonal antibody generated by immunizing BALB/c mice with the specified immunogen and fusing splenocytes with P3-AgX-653 myeloma cells (see application references). Recognizes the ~94-97 kDa glucocorticoid receptor.
BackgroundSteroids regulate important neuronal functions including the organization of neural circuits during development and the regulation of synapse organization in the adult. Steroid hormones may promote cell survival and differentiation of both neurons and glial cells, regulate synaptogenesis, prevent synapse elimination, cause axonal and dendritic growth, and play a role during regeneration of the nervous system. Steroid hormone receptors are members of a large family of nuclear ligand-activated transcription factors that includes the androgen, estrogen, glucocorticoid, and progesterone receptors. In the absence of hormone, steroid receptors are associated in complexes with heat shock proteins and immunophilins. Steroid binding results in the dissociation of the heat-shock protein, receptor dimerization, and binding to specific hormone response elements (HRE) to produce a transcriptionally active complex that leads to the activation or repression of target genes. Steroid receptors are regulated by phosphorylation, however, modulation of kinase activity can also cause receptor activation in the absence of hormone. Recent evidence suggests that steroid receptor expression can be regulated by neurotrophins, and that steroids can regulate the expression of trophic factors and their receptors.
HostMouse
Immunogen speciesRat
Immunogenpartially purified, rat glucocorticoid receptor
CloneBuGR2
IsotypeIgG2a
Speciesnot amphibian, not avian, guinea pig, mouse, not primate, rabbit, rat, sheep
Positive controlmouse liver extract
FormLyophilized
FormulationLyophilized from PBS, pH 7.2.
Preservative≤0.1% sodium azide
CommentsDoes not cross react with androgen, progesterone, estrogen or mineralocorticoid receptors. Enzymatic digestion and immunoblot analysis has shown that this antibody reacts with the undigested 97 kDa glucocorticoid receptor, a 17 kDa DNA-binding trypsin fragment, and a 45 kDa steroid and DNA-binding chymotrypsin fragment. Immunocytochemical localization of the glucocorticoid receptor is observed in the cytoplasm and nucleus, even in the presence of hormone. This antibody has also been reported to work for immunoprecipitation. Antibody should be titrated for optimal results in individual systems.
Storage -20°C
Do Not Freeze Ok to freeze
Special InstructionsResuspend the lyophilized antibody with 0.1 ml sterile PBS, pH 7.2. Be careful to reconstitute the entire contents of the vial; during shipment and handling, portions of the lyophilized pellet may have become dislodged and may not be in the bottom of the vial. Following reconstitution, aliquot and freeze (-20°C). Avoid freeze/thaw cycles of solutions.
Toxicity Standard Handling
ReferencesHussien, A., et al. 1997. Proc. Natl. Acad. Sci. USA 94, 1521.
Pratt, W.B. and Toft, D.O., 1997. Endocrine Rev. 18 306.
Schumacher, M., et al. 1996. Dev. Neurosci. 18, 6.
Toran-Allerand, C.D. 1996. Dev. Neurosci. 18, 36.
Weigel, N.L. 1996. Biochem J. 319, 657.
Jones, K.J. 1994. Ann. N.Y. Acad. Sci. 743, 141.
Arnold, A.P. 1990. in Hormones, Brain and Behavior in Vertebrates, ed. Balthazart, J. (Karger, Basel), 82.
Application referencesOriginal Clone Gametchu, B. and Harrison, R., 1984. Endocrinology 114, 274.