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LMX1B antibody (AA 136-395)

This anti-LMX1B antibody is a Rabbit Polyclonal antibody detecting LMX1B in WB. Suitable for Human.
Catalog No. ABIN6143280

Quick Overview for LMX1B antibody (AA 136-395) (ABIN6143280)

Target

See all LMX1B Antibodies
LMX1B (LIM Homeobox Transcription Factor 1, beta (LMX1B))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This LMX1B antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 136-395

    Sequence

    YHLGCFCCCV CERQLRKGDE FVLKEGQLLC KGDYEKEKDL LSSVSPDESD SVKSEDEDGD MKPAKGQGSQ SKGSGDDGKD PRRPKRPRTI LTTQQRRAFK ASFEVSSKPC RKVRETLAAE TGLSVRVVQV WFQNQRAKMK KLARRHQQQQ EQQNSQRLGQ EVLSSRMEGM MASYTPLAPP QQQIVAMEQS PYGSSDPFQQ GLTPPQMPGN DSIFHDIDSD TSLTSLSDCF LGSSDVGSLQ ARVGNPIDRL YSMQSSYFAS

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 136-395 of human LMX1B (NP_002307.2).

    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

    LMX1B (LIM Homeobox Transcription Factor 1, beta (LMX1B))

    Alternative Name

    LMX1B

    Background

    This gene encodes a member of LIM-homeodomain family of proteins containing two N-terminal zinc-binding LIM domains, 1 homeodomain, and a C-terminal glutamine-rich domain. It functions as a transcription factor, and is essential for the normal development of dorsal limb structures, the glomerular basement membrane, the anterior segment of the eye, and dopaminergic and serotonergic neurons. Mutations in this gene are associated with nail-patella syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.,LMX1B,LMX1.2,NPS1,Epigenetics & Nuclear Signaling,Transcription Factors,Neuroscience,Neurodegenerative Diseases,Dopamine Signaling in Parkinson's Disease,LMX1B

    Molecular Weight

    44 kDa/45 kDa

    Gene ID

    4010

    UniProt

    O60663

    Pathways

    Dopaminergic Neurogenesis
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