PIMA526678

POMK Monoclonal Antibody (OTI2B10), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA526678-Each-of-1 In Stock ₹ 52,198.50

PIMA526678 - Each of 1

₹ 52,198.50

In Stock

Quantity

1

Base Price: ₹ 52,198.50

GST (18%): ₹ 9,395.73

Total Price: ₹ 61,594.23

Antigen

POMK

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

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

Gene Accession No.

Q9H5K3

Gene Symbols

POMK

Immunogen

Human recombinant protein fragment corresponding to amino acids 141-350 of SGK196 produced in E.coli

Quantity

100μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG1

Applications

Immunohistochemistry (Paraffin), Western Blot

Clone

OTI2B10

Conjugate

Unconjugated

Gene

POMK

Gene Alias

4930444A02Rik; MDDGA12; MDDGC12; Pomk; probable inactive protein kinase-like protein SgK196; protein kinase-like protein SgK196; protein kinase-like protein SgK196-like; protein O-mannose kinase; protein-O-mannose kinase; RGD1310810; SGK196; sugen kinase 196

Host Species

Mouse

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

84197

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Related Products

Img

Novus Biologicals

NBP272275B

--

Img

Novus Biologicals

NBP272275IR

--

Img

Thermo Scientific

PIPA530729

--

Img

Thermo Scientific

PA550128

--

Img

Thermo Scientific

PIPA584414

--

Img

Thermo Scientific

PIPA527612

--

Img

Thermo Scientific

PIPA582512

--

Img

Thermo Scientific

PIMA525998

--

Description

  • This gene encodes a protein that may be involved in the presentation of the laminin-binding O-linked carbohydrate chain of alpha-dystroglycan (a-DG), which forms transmembrane linkages between the extracellular matrix and the exoskeleton
  • Some pathogens use this O-linked carbohydrate unit for host entry
  • Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype
  • Mice lacking this gene contain misplaced neurons (heterotopia) in some regions of the brain, possibly from defects in neuronal migration
  • Alternative splicing of this gene results in multiple transcript variants.