SGK196 antibody (AA 1-350)

Catalog No. ABIN7269648

The Rabbit Polyclonal anti-SGK196 antibody (ABIN7269648) specifically detects SGK196 in WB. The antibody is reactive with Human samples.

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

Target: SGK196 (Protein Kinase Protein SgK196 (SGK196))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SGK196 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-SGK196 Antibody

Binding Specificity: 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 Details

Application Notes: WB,1:200 - 1:2000

Restrictions: For Research Use only

Handling

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 Details for SGK196

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