PIMA514719

Hemoglobin Monoclonal Antibody (9A5), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA514719-Each-of-1 In Stock ₹ 43,654.50

PIMA514719 - Each of 1

₹ 43,654.50

In Stock

Quantity

1

Base Price: ₹ 43,654.50

GST (18%): ₹ 7,857.81

Total Price: ₹ 51,512.31

Antigen

Hemoglobin

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with 1mg/mL BSA and 0.05% sodium azide; pH 7.4

Gene Accession No.

P68871, P69905

Gene Symbols

HBA1, HBB

Immunogen

Human Hemoglobin

Quantity

100 μg

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

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Description

  • MA5-14719 targets Hemoglobin in ELISA, IP, and RIA applications and shows reactivity with Human samples
  • The MA5-14719 immunogen is human Hemoglobin
  • MA5-14719 detects Hemoglobin which has a predicted molecular weight of approximately 15 kDa
  • Product MA514719 is a smaller package size of MIH9506 (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.