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Rabbit anti-Human LBR Polyclonal Antibody

The antibody against LBR was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-211 of human LBR (NP_002287.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

ADA-08782A

The antibody against LBR was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-211 of human LBR (NP_002287.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

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Specifications


Cat.No ADA-08782A ClonalityPolyclonal
Host SpeciesRabbitTarget NameLBR
Target SynonymsPHA; C14SR; LMN2R; PHASK; TDRD18; DHCR14B; LBRFormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive Samples22Rv1, Mouse eye, Mouse lung, Mouse spleenApplicationELISA, WB, IF/ICC

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-211 of human LBR (NP_002287.2).Target SpeciesHuman
Uniprot IDQ14739Immunogen Sequence
Background Information
  • Uniprot Id

    Q14739

  • Target Species

    Human

  • Target Name

    LBR

  • Target Full Name

    Delta(14)-sterol reductase LBR

  • Target Function

    Catalyzes the reduction of the C14-unsaturated bond of lanosterol, as part of the metabolic pathway leading to cholesterol biosynthesis. Plays a critical role in myeloid cell cholesterol biosynthesis which is essential to both myeloid cell growth and functional maturation. Mediates the activation of NADPH oxidases, perhaps by maintaining critical levels of cholesterol required for membrane lipid raft formation during neutrophil differentiation. Anchors the lamina and the heterochromatin to the inner nuclear membrane.

  • Target Involvement

    Pelger-Huet anomaly (PHA); Greenberg dysplasia (GRBGD); Reynolds syndrome (REYNS)

  • Target Subcellular Location

    Nucleus inner membrane; Multi-pass membrane protein. Endoplasmic reticulum membrane. Cytoplasm. Nucleus.

  • Target Protein Families

    ERG4/ERG24 family

  • Target Tissue Specificity

    Expressed in the bone marrow, liver, heart, adrenal gland, lung, placenta and uterus. Expressed in osteoclasts and osteoblast-like cells.

  • Target Synonyms

    DHCR 14B; DHCR14B; Integral nuclear envelope inner membrane protein; Lamin-B receptor; LBR; LBR_HUMAN; LMN 2R; LMN2R; MGC9041; PHA; PRO0650

  • Target Background

    The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified.

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