Rat hypoxia-inducible factor 1α,HIF-1α ELISA Kit

SKU:BHE10508142
Overview
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Quantitative ELISA kit for measuring rat hypoxia-inducible factor 1α (HIF1A) in serum, plasma, and tissue homogenates to support epigenetics and nuclear signaling studies. Sensitivity 0.78 pg/mL, detection range 3.12 pg/mL–200 pg/mL, typical assay time 1–5 h.
Target HIF
Species Rattus norvegicus (Rat)
Sample Type(s) serum, plasma, tissue homogenates
Assay Type Sandwich ELISA (quantitative)
Sensitivity 0.78 pg/mL
Detection Range 3.12 pg/mL-200 pg/mL
Assay Time 1-5h
Options selector
Catalog no. Size
CSB-E08540r-96T 96 T
CSB-E08540r-96TX5 96 T×5
CSB-E08540r-96TX10 96 T×10
Available Options

Select from the available variant options shown for this product. Availability and lead time can vary by option.

  • Options: Size (96 T, 96 T×10, 96 T×5).
  • Lead time: options listed as "In Stock at Manufacturer" typically ship in 5–7 business days; other statuses may take longer.
  • Storage: refer to the product datasheet for storage and handling.
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Field Specification
Target HIF
Alternative names Hif1aHypoxia-inducible factor 1-alpha ELISA Kit; HIF-1-alpha ELISA Kit; HIF1-alpha ELISA Kit
UniProt # O35800
Species Rattus norvegicus (Rat)
Reactivity
  • Rat
Applications
  • ELISA
Assay type
  • Sandwich ELISA (quantitative)
Sample type(s) serum, plasma, tissue homogenates
Sensitivity 0.78 pg/mL
Detection range 3.12 pg/mL-200 pg/mL
Detection wavelength 450 nm
Assay time
  • 1-5h
Catalog no. (Mfr.) CSB-E08540r
Main SKU BHE10508142

Background

hypoxia-inducible factor 1α (HIF1A) is a biological molecule commonly studied in epigenetics and nuclear signaling research. It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.

UniProt: O35800

Biological context

Researchers often monitor hypoxia-inducible factor 1α in serum, plasma, and tissue homogenates to better understand themes such as mechanistic biology studies, biomarker-focused profiling, and disease-model research. In many model systems, measured levels can shift with physiology, experimental perturbation, or disease-associated changes, making careful biological interpretation important.

Interpreting changes in measured levels

Depending on sample matrix and study design, increases or decreases in hypoxia-inducible factor 1α may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. Interpretation is typically strengthened by evaluating related molecules (for example, complementary pathway markers and controls appropriate to the biological model) and by keeping pre-analytical variables consistent across groups.

Nomenclature

In publications and databases, hypoxia-inducible factor 1α may also appear under names such as Hif1aHypoxia-inducible factor 1-alpha and HIF-1-alpha. When comparing studies, confirm that the reported analyte refers to the same molecule and species context.

Why ELISA data are widely used

ELISA is a common approach for quantitative measurement of proteins and biomarkers in complex samples, enabling comparisons across experimental groups and time points. When integrating results with other readouts, consider species biology, sample type, and the broader pathway context that hypoxia-inducible factor 1α participates in.

Can’t Find What You’re Looking For? We can help you source the best match or customize an ELISA solution for your study. Options may include alternative target synonyms, different species reactivity, sample type/matrix compatibility (serum/plasma/lysate/supernatant), assay format (sandwich/competitive), sensitivity/range, detection chemistry (colorimetric/fluorescent/chemiluminescent), plate format (pre-coated/uncoated, strips vs full plate), and bulk or custom packaging. Click Talk to a Scientist to submit a request form, email us at support@biohippo.com, or explore our Research Services for additional support. Our team will be in contact with you shortly.

SEX DIFFERENCES IN SYSTEMIC INFLAMMATORY RESPONSE IN LOW HYPOXIA-RESISTANT RATS

I Tsvetkov, A Kosyreva, D Dzhalilova, O Makarova,Morphology,2024

Boosting effects of Cranberry and Cinnamaldehyde for pioglitazone amelioration of liver steatosis in rat via suppression of HIF-1α/Smad/β-catenin signaling

MA Ali,Journal of Functional Foods,2023

Oxygen-Glucose Deprivation in Organotypic Hippocampal Cultures Leads to Cytoskeleton Rearrangement and Immune Activation: Link to the Potential Pathomechanism of Ischaemic Stroke

N Bryniarska-Kubiak,Cells,2023

Cubic multi-ions-doped Na2TiO3 nanorod-like coatings: Structure-stable, highly efficient platform for ions-exchanged release to immunomodulatory promotion on vascularized bone apposition

Dongmei Yu,Bioactive Materials,2022

Assessment of the effects of ischaemia/hypoxia on angiogenesis in rat myofascial trigger points using colour Doppler flow imaging

F Jiang,PeerJ,2020

Short-term exercise training improves cardiac function associated to a better antioxidant response and lower type 3 iodothyronine deiodinase activity after myocardial infarction

Marschner RA, et al,Plos One,2019

A Promising Approach to Integrally Evaluate the Disease Outcome of Cerebral Ischemic Rats Based on Multiple-Biomarker Crosstalk

Guimei Ran.et al,DiseaseMarkers,2017

Expression and specific activities of carbamoyl phosphate synthetase 1 in chronic hypoxic rats

Nikmah U A.et al,Medical Journal of Indonesia,2016

Measurement of levels of lung HIF-1伪 protein in response to tapering for 14- and 21-day with nigella sativa supplementation in maturing rat, with histological study

Ehsan Arabzadeh.et al,Sport Sciences for Health,2015

Influence of thyroid state on cardiac and renal capillary density and glomerular morphology in rats

Rodriacuteguez-Goacutemez I et al,J Endocrinol,2013

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