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SGK196 antibody (AA 1-350)

This anti-SGK196 antibody is a Rabbit Polyclonal antibody detecting SGK196 in WB. Suitable for Human.
Catalog No. ABIN7269648

Quick Overview for SGK196 antibody (AA 1-350) (ABIN7269648)

Target

See all SGK196 Antibodies
SGK196 (Protein Kinase Protein SgK196 (SGK196))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This SGK196 antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 1-350

    Purpose

    POMK Rabbit pAb

    Sequence

    MEKQPQNSRR GLAPREVPPA VGLLLIMALM NTLLYLCLDH FFIAPRQSTV DPTHCPYGHF RIGQMKNCSP WLSCEELRTE VRQLKRVGEG AVKRVFLSEW KEHKVALSQL TSLEMKDDFL HGLQMLKSLQ GTHVVTLLGY CEDDNTMLTE YHPLGSLSNL EETLNLSKYQ NVNTWQHRLE LAMDYVSIIN YLHHSPVGTR VMCDSNDLPK TLSQYLLTSN FSILANDLDA LPLVNHSSGM LVKCGHRELH GDFVAPEQLW PYGEDVPFHD DLMPSYDEKI DIWKIPDISS FLLGHIEGSD MVRFHLFDIH KACKSQTPSE RPTAQDVLET YQKVLDTLRD AMMSQAREML

    Cross-Reactivity

    Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-350 of human POMK (NP_115613.1).

    Isotype

    IgG
  • Application Notes

    WB,1:200 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    SGK196 (Protein Kinase Protein SgK196 (SGK196))

    Alternative Name

    POMK

    Background

    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.,POMK,MDDGA12,MDDGC12,SGK196,Signal Transduction,Kinase,POMK

    Molecular Weight

    40kDa

    Gene ID

    84197

    UniProt

    Q9H5K3
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