MA143012

Factor IX Monoclonal Antibody (5041), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 MA143012-Each-of-1 In Stock ₹ 43,031.50

MA143012 - Each of 1

₹ 43,031.50

In Stock

Quantity

1

Base Price: ₹ 43,031.50

GST (18%): ₹ 7,745.67

Total Price: ₹ 50,777.17

Antigen

Factor IX

Classification

Monoclonal

Concentration

9.5 mg/mL

Formulation

50% water with 50% glycerol and no preservative

Gene Accession No.

P00740

Gene Symbols

F9

Immunogen

Heavy chain of human factor IX and Ixa.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG1

Applications

ELISA, Immunohistochemistry, Radioimmune Assays (RIA), Western Blot

Clone

5041

Conjugate

Unconjugated

Gene

F9

Gene Alias

AW111646; Cf9; Cf-9; Christmas factor; coagulation factor 9; coagulation factor IX; coagulation factor IX (plasma thromboplastic component, Christmas disease, hemophilia B); Coagulation factor IXa heavy chain; Coagulation factor IXa light chain; EC 3.4.21.22; F9; F9 p22; factor 9; factor IX (Christmas factor) precursor; factor IX F9; Factor9; FIX; FIX F9; HEMB; P19; plasma thromboplastic component; plasma thromboplastin component; PTC; RP6-88D7.1; serine protease; THPH8

Host Species

Mouse

Purification Method

Affinity chromatography, Ammonium sulfate precipitation

Regulatory Status

RUO

Gene ID (Entrez)

2158

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • MA1-43012 detects Factor IX in human samples, human factor Ixa and the heavy chain of human factor IX and IXa
  • MA1-43012 has successfully been used in radioimmune assays, ELISA, Western blot and immunohistochemistry applications
  • MA1-43012 was derived from human factor IX
  • Coagulation factor IX is a single chain polypeptide with a molecular mass of 57 kDa
  • Normal concentrations of factor IX in human plasma is approximately 3 μg/mL
  • Factor IX deficiency and lack of coagulation activity is seen in patients suffering from the innate X-chromosome linked disorder, haemophilia B.