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GPD1L antibody (AA 1-351)

The Rabbit Polyclonal anti-GPD1L antibody has been validated for WB. It is suitable to detect GPD1L in samples from Human.
Catalog No. ABIN7267460

Quick Overview for GPD1L antibody (AA 1-351) (ABIN7267460)

Target

See all GPD1L Antibodies
GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This GPD1L antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 1-351

    Purpose

    GPD1L Rabbit pAb

    Sequence

    MAAAPLKVCI VGSGNWGSAV AKIIGNNVKK LQKFASTVKM WVFEETVNGR KLTDIINNDH ENVKYLPGHK LPENVVAMSN LSEAVQDADL LVFVIPHQFI HRICDEITGR VPKKALGITL IKGIDEGPEG LKLISDIIRE KMGIDISVLM GANIANEVAA EKFCETTIGS KVMENGLLFK ELLQTPNFRI TVVDDADTVE LCGALKNIVA VGAGFCDGLR CGDNTKAAVI RLGLMEMIAF ARIFCKGQVS TATFLESCGV ADLITTCYGG RNRRVAEAFA RTGKTIEELE KEMLNGQKLQ GPQTSAEVYR ILKQKGLLDK FPLFTAVYQI CYESRPVQEM LSCLQSHPEH T

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-351 of human GPD1L (NP_055956.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 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

    GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

    Alternative Name

    GPD1L

    Background

    The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).,GPD1L,GPD1-L,Cancer,Signal Transduction,Cell Biology & Developmental Biology,Endocrine & Metabolism,GPD1L

    Molecular Weight

    38kDa

    Gene ID

    23171

    UniProt

    Q8N335
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