ProSci

IRE1p Antibody

Product Code:
 
PSI-3657
Product Group:
 
Primary Antibodies
Supplier:
 
ProSci
Host Type:
 
Rabbit
Antibody Isotype:
 
IgG
Antibody Clonality:
 
Polyclonal
Regulatory Status:
 
RUO
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Immunofluorescence (IF)
  • Immunohistochemistry (IHC)
  • Western Blot (WB)
1 / 3
Western blot analysis of IRE1p in A-20 cell lysate with IRE1p antibody at (A) 0.5, (B) 1 and (C) 2 μg/mL.
2 / 3
Immunocytochemistry of IRE1p in A20 cells with IRE1p antibody at 1 μg/mL.
3 / 3
Immunofluorescence of IRE1p in A20 cells with IRE1p antibody at 10 μg/mL.

Western blot analysis of IRE1p in A-20 cell lysate with IRE1p antibody at (A) 0.5, (B) 1 and (C) 2 μg/mL.
Immunocytochemistry of IRE1p in A20 cells with IRE1p antibody at 1 μg/mL.
Immunofluorescence of IRE1p in A20 cells with IRE1p antibody at 10 μg/mL.

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CodeSizePrice
PSI-3657-0.02mg0.02mg£150.00
Quantity:
PSI-3657-0.1mg0.1mg£449.00
Quantity:
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This product comes from: United States.
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Further Information

Additional Names:
IRE1p Antibody: IRE1, IRE1P, IRE1a, hIRE1p, IRE1, Endoplasmic reticulum-to-nucleus signaling 1
Application Note:
IRE1p antibody can be used for the detection of IRE1p by Western blot at 0.5 - 2 μg/mL. Antibody can also be used for immunocytochemistry starting at 1 μg/mL. For immunofluorescence start at 10 μg/mL.

Antibody validated: Western Blot in mouse samples; Immunocytochemistry in mouse samples and Immunofluorescence in mouse samples. All other applications and species not yet tested.
Background:
IRE1p Antibody: Accumulation of malfolded proteins in the endoplasmic reticulum (ER) activates the unfolded protein response (UPR) and the upregulation of the ER molecular chaperones GRP78 and GRP 94. These proteins are normally bound to ER transmembrane proteins such as IRE1p and ATF6 but ER stress causes their dissociation. This allows IRE1p, a serine-threonine protein kinase to transduce the unfolded protein signal from the ER to the nucleus. IRE1p also has an endoribonuclease activity that is required to splice X-box binding protein (XBP1) mRNA converting it to a potent UPR transcriptional activation. Depletion of IRE1p through the expression of a dominant negative form of IRE1p has no effect on transfected cells, but cell death via apoptosis occurs under stress conditions that cause unfolded proteins to accumulate in the ER. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Background References:
  • Little E, Ramakrishnan M, Roy B, et al. The glucose-regulated proteins (GRP78 and GRP94): functions, gene regulation, and applications. Crit. Rev. Eukaryot. Gene Expr.1994; 4:1-18.
  • Lee AS. The ER chaperone and signaling regulator GRP78/BiP as a monitor of endoplasmic reticulum stress. Methods2005; 35:373-81.
  • Bertolotti A, Zhang Y, Hendershot LM, et al. Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response. Nat. Cell Biol.2000; 2:326-32.
  • Shen J, Chen X, Hendershot L, et al. ER stress regulation of ATF6 localization by dissociation of BiP/GRP78 binding and unmasking of Golgi localization signals. Dev. Cell2002; 3:99-111.
Buffer:
IRE1p Antibody is supplied in PBS containing 0.02% sodium azide.
Concentration:
1 mg/mL
Conjugate:
Unconjugated
DISCLAIMER:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.
Immunogen:
IRE1p antibody was raised against a 15 amino acid synthetic peptide from near the amino terminus of human IRE1p.

The immunogen is located within amino acids 150 - 200 of IRE1p.
NCBI Gene ID #:
2081
NCBI Official Name:
endoplasmic reticulum to nucleus signaling 1
NCBI Official Symbol:
ERN1
NCBI Organism:
Homo sapiens
Physical State:
Liquid
Protein Accession #:
O75460
Protein GI Number:
193806335
Purification:
IRE1p Antibody is affinity chromatography purified via peptide column.
Research Area:
Signal Transduction,
Swissprot #:
O75460
User NOte:
Optimal dilutions for each application to be determined by the researcher.