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Rabbit IgG (H&L) Antibody Peroxidase Conjugated
Donkey Polyclonal
12 References
611-7302
2 mg
Lyophilized
WB, ELISA
Rabbit
Donkey
Shipping info:
$50.00 to US & $70.00 to Canada for most products. Final costs are calculated at checkout.
Product Details
Donkey Anti-Rabbit IgG (H&L) Antibody Peroxidase Conjugated - 611-7302
Donkey anti-Rabbit IgG Peroxidase Conjugated Antibody, Donkey anti-Rabbit IgG Antibody HRP Conjugation
Donkey
IgG (H&L)
Peroxidase (HRP)
Polyclonal
IgG
Target Details
Rabbit
Native Protein
Anti-Rabbit IgG (H&L) was produced by repeated immunization with rabbit whole IgG molecule in donkey.
This product was prepared from monospecific antiserum by immunoaffinity chromatography using Rabbit IgG coupled to agarose beads. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Peroxidase, anti-Donkey Serum, Rabbit IgG and Rabbit Serum.
Application Details
ELISA, WB
Anti-Rabbit IgG peroxidase conjugated antibody has been tested by ELISA and western blot and is suitable for immunoblotting (western or dot blot), ELISA, immunoperoxidase electron microscopy and immunohistochemistry as well as other peroxidase-antibody based enzymatic assays requiring lot-to-lot consistency.
Formulation
2.0 mg/mL by UV absorbance at 280 nm
0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
0.01% (w/v) Gentamicin Sulfate. Do NOT add Sodium Azide!
10 mg/mL Bovine Serum Albumin (BSA) - Immunoglobulin and Protease free
1.0 mL
Restore with deionized water (or equivalent)
Shipping & Handling
Ambient
Store vial at 4° C prior to restoration. For extended storage aliquot contents and freeze at -20° C or below. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.
Expiration date is one (1) year from date of receipt.
Anti-Rabbit IgG (H&L) peroxidase Antibody generated in donkey detects reactivity to Rabbit IgG. Secreted as part of the adaptive immune response by plasma B cells, immunoglobulin G constitutes 75% of serum immunoglobulins. Immunoglobulin G binds to viruses, bacteria, as well as fungi and facilitates their destruction or neutralization via agglutination (and thereby immobilizing them), activation of the compliment cascade, and opsinization for phagocytosis. The whole IgG molecule possesses both the F(c) region, recognized by high-affinity Fc receptor proteins, as well as the F(ab) region possessing the epitope-recognition site. Both the Heavy and Light chains of the antibody molecule are present. Secondary Antibodies are available in a variety of formats and conjugate types. When choosing a secondary antibody product, consideration must be given to species and immunoglobulin specificity, conjugate type, fragment and chain specificity, level of cross-reactivity, and host-species source and fragment composition.
Eiger DS et al. (2023). Phosphorylation barcodes direct biased chemokine signaling at CXCR3. Cell Chem Biol.
Applications
WB, IB, PCA
Hörner C et al. (2023). A protective measles virus-derived vaccine inducing long-lasting immune responses against influenza A virus H7N9. NPJ Vaccines.
Applications
WB, IB, PCA
Eiger DS et al. (2022). Location bias contributes to functionally selective responses of biased CXCR3 agonists. Nat Commun.
Applications
WB, IB, PCA
Papenfuss M et al. (2022). Differential maturation and chaperone dependence of the paralogous protein kinases DYRK1A and DYRK1B. Sci Rep.
Applications
WB, IB, PCA
Hossain D et al. (2020). Requirement of NPHP5 in the hierarchical assembly of basal feet associated with basal bodies of primary cilia. Cell Mol Life Sci.
Applications
WB, IB, PCA
Hossain D et al. (2020). Cep44 functions in centrosome cohesion by stabilizing rootletin. J Cell Sci.
Applications
WB, IB, PCA
Hanauer JR et al. (2019). High-affinity DARPin allows targeting of MeV to glioblastoma multiforme in combination with protease targeting without loss of potency. Mol Ther Oncolytics.
Applications
WB, IB, PCA
Hossain D et al. (2018). HIV-1 Vpr hijacks EDD-DYRK2-DDB1DCAF1 to disrupt centrosome homeostasis. J Biol Chem.
Applications
WB, IB, PCA
Liu X et al. (2018). Acetate production from glucose and coupling to mitochondrial metabolism in mammals. Cell.
Applications
WB, IB, PCA
Liberti et al. (2017). A Predictive Model for Selective Targeting of the Warburg Effect through GAPDH Inhibition with a Natural Product. Cell Metabolism
Applications
WB, IB, PCA
Wu Q et al. (2017). Blocking beta 2-adrenergic receptor inhibits dendrite ramification in a mouse model of Alzheimer's disease. Neural Regeneration Research
Applications
WB, IB, PCA
Hu X et al. (2016). Resveratrol induces cell cycle arrest and apoptosis in human eosinophils from asthmatic individuals. Mol Med Rep.
Applications
WB, IB, PCA
This product is for research use only and is not intended for therapeutic or diagnostic applications. Please contact a technical service representative for more information. All products of animal origin manufactured by Rockland Immunochemicals are derived from starting materials of North American origin. Collection was performed in United States Department of Agriculture (USDA) inspected facilities and all materials have been inspected and certified to be free of disease and suitable for exportation. All properties listed are typical characteristics and are not specifications. All suggestions and data are offered in good faith but without guarantee as conditions and methods of use of our products are beyond our control. All claims must be made within 30 days following the date of delivery. The prospective user must determine the suitability of our materials before adopting them on a commercial scale. Suggested uses of our products are not recommendations to use our products in violation of any patent or as a license under any patent of Rockland Immunochemicals, Inc. If you require a commercial license to use this material and do not have one, then return this material, unopened to: Rockland Inc., P.O. BOX 5199, Limerick, Pennsylvania, USA.
