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Hemoglobin Subtype Analysis by Electrophoresis (Serum/Plasma)

Published: August 9, 2026Updated: August 16, 2026

This test measures different types of hemoglobin in your blood, which can help identify conditions like sickle cell disease or other hemoglobinopathies.

Quick summary

["This test helps diagnose blood disorders by checking for unusual hemoglobin patterns."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
6864-3
Short code
Hgb S Bld Ql Soly
Synonyms
Hgb S Bld Ql Soly
Category
hematology
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Ref low
12
Ref high
17.5
Critical range
7 N/A – 20 N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
solubility-test
CPT
85018
SNOMED
900000000000003004
Specimen volume
3 mL
Stability
Room temperature: 4h, Refrigerated: 24h
Hemolysis max
0
Lipemia max
0
Icterus max
0
TAT
4–24 hours
Order
routine

What This Test Measures

Hemoglobin is the protein in red blood cells that carries oxygen. Certain genetic conditions cause variations in hemoglobin structure, which this test detects. The electrophoresis method separates hemoglobin types based on their electrical charge, revealing any abnormal forms.

Why It’s Done

Your healthcare provider may order this test if you have symptoms like fatigue, pain, or frequent infections, or if you have a family history of blood disorders. It’s also used in newborn screening for conditions like sickle cell anemia.

Sample Collection and Preparation

A blood sample is taken from a vein, usually in your arm. The blood is processed to separate serum or plasma, where hemoglobin types are analyzed using an electrophoresis technique that sorts proteins by size and charge.

What to Expect Before the Test

No special preparation is needed, but inform your provider about any medications or recent blood transfusions. Avoid strenuous activity 24 hours before testing if possible.

Reference range

Adult males: 13.5-17.5 g/dL; Females: 12.0-16.0 g/dLN/A

Specimen: whole-blood

No special preparation usually required. Stay well hydrated. Inform your healthcare provider of all medications and supplements you are taking.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Abnormal hemoglobin patterns may indicate genetic disorders like sickle cell disease, thalassemia, or other hemoglobinopathies. Early detection can guide treatment and management strategies, such as monitoring, medication, or lifestyle adjustments.

Short name

Hb Subtype Screening

Frequently asked questions

What does an abnormal result mean?
An abnormal result may suggest an inherited blood disorder that affects how your red blood cells carry oxygen. Your provider will discuss findings with you and may recommend further testing or follow-up.
How long does it take to get results?
Results are typically available within 24 to 48 hours, depending on lab processing times. Follow-up with your healthcare provider is important to interpret results and plan next steps.
Can I fast before this test?
No fasting is required for this test, as it involves a blood sample without dietary restrictions.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy