Hemoglobin alpha-1 Monoclonal Antibody (C6), Invitrogen™
Manufacturer: Fischer Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA550889-Each-of-1 | In Stock | ₹ 46,769.50 |
FEMA550889 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,769.50
GST (18%): ₹ 8,418.51
Total Price: ₹ 55,188.01
Antigen
Hemoglobin alpha-1
Classification
Monoclonal
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.05% Proclin 300, pH 7.4
Gene Accession No.
P01946, P69905
Gene Symbols
HBA1
Immunogen
Recombinant Human HBa1 protein, Met1-Arg142 (Accession #P69905)
Quantity
200 μL
Primary or Secondary
Primary
Target Species
Human, Rat
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Clone
C6
Conjugate
Unconjugated
Gene
HBA1
Gene Alias
alpha one globin, alpha-2 globin chain, Alpha-globin, delta globin, HBA1, HBA2, HBA-T3, HBH, hemoglobin alpha 1 globin chain, Hemoglobin alpha chain, Hemoglobin subunit alpha, hemoglobin subunit alpha 1, hemoglobin, alpha 1
Host Species
Mouse
Purification Method
Protein A/G
Regulatory Status
RUO
Gene ID (Entrez)
25632, 3039
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Isotype
IgG1 κ
Related Products
Description
- The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'
- The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical
- These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions
- Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin
- Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported.