PIPA5121925

Hemoglobin alpha-1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5121925-Each-of-1 In Stock ₹ 19,669.00

PIPA5121925 - Each of 1

₹ 19,669.00

In Stock

Quantity

1

Base Price: ₹ 19,669.00

GST (18%): ₹ 3,540.42

Total Price: ₹ 23,209.42

Antigen

Hemoglobin alpha-1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Hba

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

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

15121

Content And Storage

-20°C

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

500 μg/mL

Formulation

PBS with 50% glycerol and 0.05% ProClin 300

Gene Accession No.

P01942

Gene Symbols

Hba

Immunogen

Recombinant protein Hemoglobin Alpha 1. The antigen corresponds to amino acid range 1-142 of the target protein.

Quantity

20 μL

Primary or Secondary

Primary

Target Species

Mouse

Product Type

Antibody

Isotype

IgG

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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.