PIMA524905

Adenylate Kinase 1 Monoclonal Antibody (OTI19D1), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA524905-Each-of-1 In Stock ₹ 52,287.50

PIMA524905 - Each of 1

₹ 52,287.50

In Stock

Quantity

1

Base Price: ₹ 52,287.50

GST (18%): ₹ 9,411.75

Total Price: ₹ 61,699.25

Antigen

Adenylate Kinase 1

Classification

Monoclonal

Concentration

1.00 mg/mL

Formulation

PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3

Gene Accession No.

P00568

Gene Symbols

AK1

Immunogen

Full length human recombinant protein of AK1 produced in HEK293T cell

Quantity

100μL

Primary or Secondary

Primary

Target Species

Human, Non-human Primate

Product Type

Antibody

Isotype

IgG2b

Applications

Flow Cytometry, Immunocytochemistry, Western Blot

Clone

OTI19D1

Conjugate

Unconjugated

Gene

AK1

Gene Alias

adenylate kinase 1; adenylate kinase isoenzyme 1; adenylate kinase isoenzyme 1 {ECO:0000255; Adenylate monophosphate kinase; adenylate monophosphate kinase {ECO:0000255; AK 1; AK 1 {ECO:0000255; Ak1; Ak-1; ATP:AMP phosphotransferase; ATP:AMP phosphotransferase {ECO:0000255; ATP-AMP transphosphorylase 1; ATP-AMP transphosphorylase 1 {ECO:0000255; B430205N08Rik; cytosolic adenylate kinase; HAMAP-Rule:MF_03171}; HTL-S-58j; I79_014777; Myokinase; myokinase {ECO:0000255; testis secretory sperm binding protein Li 58j

Host Species

Mouse

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

203

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • Adenylate kinase is an enzyme involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate group among adinine nucleotides
  • Three isozymes of adenylate kinase have been identified in vertebrates, adenylate isozyme 1 (AK1), 2 (AK2) and 3 (AK3)
  • AK1 is found in the cytosol of skeletal muscle, brain and erythrocytes, whereas AK2 and AK3 are found in the mitochondria of other tissues including liver and heart
  • AK1 was identified because of its association with a rare genetic disorder causing nonspherocytic hemolytic anemia where a mutation in the AK1 gene was found to reduce the catalytic activity of the enzyme.