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SGCE antibody (AA 1-317)

This anti-SGCE antibody is a Rabbit Polyclonal antibody detecting SGCE in WB. Suitable for Human.
Catalog No. ABIN6147703

Quick Overview for SGCE antibody (AA 1-317) (ABIN6147703)

Target

See all SGCE Antibodies
SGCE (Sarcoglycan, epsilon (SGCE))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This SGCE antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 1-317

    Sequence

    MQLPRWWELG DPCAWTGQGR GTRRMSPATT GTFLLTVYSI FSKVHSDRNV YPSAGVLFVH VLEREYFKGE FPPYPKPGEI SNDPITFNTN LMGYPDRPGW LRYIQRTPYS DGVLYGSPTA ENVGKPTIIE ITAYNRRTFE TARHNLIINI MSAEDFPLPY QAEFFIKNMN VEEMLASEVL GDFLGAVKNV WQPERLNAIN ITSALDRGGR VPLPINDLKE GVYVMVGADV PFSSCLREVE NPQNQLRCSQ EMEPVITCDK KFRTQFYIDW CKISLVDKTK QVSTYQEVIR GEGILPDGGE YKPPSDSLKS RDYYTDF

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-317 of human SGCE (NP_003910.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    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

    SGCE (Sarcoglycan, epsilon (SGCE))

    Alternative Name

    SGCE

    Background

    This gene encodes the epsilon member of the sarcoglycan family. Sarcoglycans are transmembrane proteins that are components of the dystrophin-glycoprotein complex, which link the actin cytoskeleton to the extracellular matrix. Unlike other family members which are predominantly expressed in striated muscle, the epsilon sarcoglycan is more broadly expressed. Mutations in this gene are associated with myoclonus-dystonia syndrome. This gene is imprinted, with preferential expression from the paternal allele. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A pseudogene associated with this gene is located on chromosome 2.,SGCE,DYT11,ESG,epsilon-SG,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,SGCE

    Molecular Weight

    49 kDa/51 kDa/52 kDa

    Gene ID

    8910

    UniProt

    O43556
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