200020149

Hemoglobin alpha-1 Monoclonal Antibody (C6), Invitrogen™

Mouse Monoclonal Antibody

Manufacturer: Fischer Scientific

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Antigen

Hemoglobin alpha-1

Concentration

1 mg/mL

Classification

Monoclonal

Form

Liquid

Regulatory Status

RUO

Formulation

PBS with 50% glycerol and 0.05% Proclin 300, pH 7.4

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

Gene Symbols

HBA1

Isotype

IgG1 κ

Purification Method

Protein A/G

Gene

HBA1

Clone

C6

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Conjugate

Unconjugated

Host Species

Mouse

Target Species

Human, Rat

Gene Accession No.

P01946, P69905

Gene ID (Entrez)

25632, 3039

Immunogen

Recombinant Human HBa1 protein, Met1-Arg142 (Accession #P69905)

Primary or Secondary

Primary

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

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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.