Goat IgG (H+L) isotype control

SKU:BHA21012541
Research Validated
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Boster Bio
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Overview
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Goat anti-Goat IgG (H+L) isotype control secondary antibody (Polyclonal). Commonly used as a detection reagent in immunoassays where secondary specificity and label choice matter.
Target Goat IgG (H+L) isotype control
Host Goat
Options selector
Catalog no. Size
BA1044-1mg 1 mg
BA1044-5mg 5 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options:
    • 1 mg; 5 mg
  • Lead time: typically ships in ~2–3 business days; timing may vary by selected option.
  • Storage: At -20℃ for one year from date of receipt. Avoid repeated freezing and thawing.
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible; avoid repeated freeze-thaw cycles.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Target Goat IgG (H+L) isotype control
Host Goat
Clonality
  • Polyclonal
Applications
  • Western Blot
Storage At -20℃ for one year from date of receipt. Avoid repeated freezing and thawing.
Catalog no. (Mfr.) BA1044
Main SKU BHA21012541
Goat Polyclonal

Product Overview

This goat polyclonal secondary antibody binds goat IgG (H+L) isotype control.

Target Goat IgG (H+L) isotype control
Host / Clonality / Isotype Goat / Polyclonal
Storage Store at −20 °C for up to 12 months from receipt. Avoid repeated freeze–thaw cycles.

Safety

For research use only; not for diagnostic or therapeutic procedures. Handle with standard laboratory precautions.
Q.What are the host species and clonality?
A.Host: Goat; clonality: Polyclonal.
Q.How should this isotype control be stored?
A.Store at −20 °C for up to 12 months from receipt. Avoid repeated freeze–thaw cycles.

Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.

Lvye Fang et al. (2021) High-Resolution Patterned Functionalization of Slippery “Liquid-Like” Brush Surfaces via Microdroplet-Confined Growth of Multifunctional Polydopamine Arrays. Advanced Functional Materials. 10.1002/adfm.202100447

Yue Du et al. (2024) Development of a bioluminescent immunoassay based on Fc-specific conjugated antibody–nanoluciferase immunoreagents for determining aflatoxin B1. Food Chemistry. 10.1016/j.foodchem.2024.141220

Yue Du et al. (2024) Fabrication of cysteine-modified antibodies with Fc-specific conjugation for covalent and oriented immobilization of native antibodies. International Journal of Biological Macromolecules. 10.1016/j.ijbiomac.2024.133962

Su Zhou et al. (2022) Low WIP1 Expression Accelerates Ovarian Aging by Promoting Follicular Atresia and Primordial Follicle Activation. Cells. 10.3390/cells11233920

Xue–Lian Hu et al. (2015) Switchable fluorescence of gold nanoclusters for probing the activity of alkaline phosphatase and its application in immunoassay. Biosensors & Bioelectronics. 10.1016/j.bios.2015.10.046

Ping Li et al. (2018) A novel strategy for amplified probing versatile biomolecules through a photoswitchable biocatalytic cascade. Sensors and Actuators B-Chemical. 10.1016/j.snb.2018.01.210

Lu-Yi Jin et al. (2015) Versatile and Amplified Biosensing through Enzymatic Cascade Reaction by Coupling Alkaline Phosphatase in Situ Generation of Photoresponsive Nanozyme. Analytical Chemistry. 10.1021/acs.analchem.5b02728

Su Zhou et al. (2017) Low expression of SEMA6C accelerates the primordial follicle activation in the neonatal mouse ovary. Journal of Cellular and Molecular Medicine. 10.1111/jcmm.13337

Yui Yamazaki et al. (2021) Involvement of multiple scavenger receptors in advanced glycation end product-induced vessel tube formation in endothelial cells. Experimental Cell Research. 10.1016/j.yexcr.2021.112857

Su Zhou et al. (2021) The inhibition of WIP1 phosphatase accelerates the depletion of primordial follicles. Reproductive Biomedicine Online. 10.1016/j.rbmo.2021.05.007

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Try Celltrypse Free – Request Your Sample Today

Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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