200020088

Hemoglobin Polyclonal Antibody, Invitrogen™

Rabbit Polyclonal Antibody

Manufacturer: Fischer Scientific

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Antigen

Hemoglobin

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Conjugate

Unconjugated

Host Species

Rabbit

Target Species

Canine, Human, Non-human Primate, Porcine

Gene Accession No.

P02067, P68871, P69905

Gene ID (Entrez)

3039, 3043, 407066

Immunogen

Native Simian HB protein (Accession #P63108;P68223)

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.

Concentration

0.5 mg/mL

Classification

Polyclonal

Form

Liquid

Regulatory Status

RUO

Formulation

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

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

Gene Symbols

HBA1, HBB

Isotype

IgG

Purification Method

Protein A

Gene

HBB

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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.