Hemoglobin alpha chain Rabbit Monoclonal Antibody(ARB968)
CAT.NO. : ARB6760
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Background
Hemoglobin alpha is the main component of human hemoglobin. Hemoglobin alpha is composed of two α globin and two β globin chains. Hemoglobin alpha chain is involved in the transport of oxygen from the lungs to various peripheral tissues.
Hemoglobin alpha is expressed in spleen, bone marrow, placenta, kidney and brain.
When hemoglobin alpha is low in the human body, it often represents a disease called beta thalassemia. Beta thalassemia is a genetic disorder caused by the loss of the beta peptide chain. There is a decrease in hemoglobin alpha, accompanied by an abnormal increase in hemoglobin F.
Hemoglobin alpha is expressed in spleen, bone marrow, placenta, kidney and brain.
When hemoglobin alpha is low in the human body, it often represents a disease called beta thalassemia. Beta thalassemia is a genetic disorder caused by the loss of the beta peptide chain. There is a decrease in hemoglobin alpha, accompanied by an abnormal increase in hemoglobin F.
Application
Application |
Dilution Ratio |
IHC |
1:100 - 1:200 |
Overview
Predicted Molecular Wt |
14kDa |
Species Cross-reactivity |
Human |
Applications |
IHC-P |
Purity |
ProA affinity purified IgG |
Form |
Liquid |
Swissprot ID |
P69905 |
Subcellular location |
Cytoplasm |
Recommended Method |
Heat induced epitope retrieval with Tris-EDTA buffer (pH 9.0), primary antibody incubate at RT (18℃-25℃) for 30 minutes |
Storage Buffer |
PBS 59%, Sodium azide 0.01%, Glycerol 40%, BSA 0.05% |
Data

Immunohistochemical staining of human breast carcinoma tissue using Hemoglobin alpha chain Rabbit Monoclonal Antibody(ARB968)
Storage
Store at -20°C. Stable for one year from the date of shipment.
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
