Hemoglobin Monoclonal Antibody (9A5), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMIH9506-Each-of-1 | In Stock | ₹ 66,349.50 |
PIMIH9506 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 66,349.50
GST (18%): ₹ 11,942.91
Total Price: ₹ 78,292.41
Antigen
Hemoglobin
Classification
Monoclonal
Concentration
5 mg/mL
Formulation
PBS with 0.09% sodium azide; pH 7.4
Gene Accession No.
P68871, P69905
Gene Symbols
HBA1, HBB
Immunogen
Human Hemoglobin
Quantity
1 mg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Applications
ELISA, Immunoprecipitation, Radioimmune Assays (RIA)
Clone
9A5
Conjugate
Unconjugated
Gene
HBB
Gene Alias
alpha one globin; alpha-1 globin; alpha-1-globin; alpha-2 globin chain; Alpha-globin; ALPHA-GLOBIN GENE; delta globin; Haemoglobin; Hb; HBA1; HbA1c; 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
Ion-exchange chromatography
Regulatory Status
RUO
Gene ID (Entrez)
3039, 3043
Content And Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C
Form
Liquid
Related Products
Description
- MIH9506 targets Hemoglobin in ELISA, IP, and RIA applications and shows reactivity with Human samples
- The MIH9506 immunogen is human Hemoglobin
- MIH9506 detects Hemoglobin which has a predicted molecular weight of approximately 15 kDa
- MIH9506 was formerly sold as a Seradyn product
- 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.