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Menin Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-72732

  • Amount:

    100ul

  • Molecular Weight:

    67993Da

  • Applications:

    WB;IHC-p;IF(paraffin section);ELISA

  • Reactivity:

    Human;Mouse;Rat

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human MEN1. AA range:181-230

  • Source:

    Polyclonal, Rabbit,IgG

  • Western Blot analysis of various cells using Menin Polyclonal Antibody diluted at 1:500

  • Gene Name:

    MEN1

  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.

  • Protein Name:

    Menin

  • Human Gene Id:

    4221

  • Human Swiss Prot No:

    O00255

  • Mouse Gene Id:

    17283

  • Mouse Swiss Prot No:

    O88559

  • Rat Gene Id:

    29417

  • Rat Swiss Prot No:

    Q9WVR8

  • Specificity:

    Menin Polyclonal Antibody detects endogenous levels of Menin protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    MEN1; SCG2; Menin

  • Observed Band(KD):

    67

  • Background:

    This gene encodes menin, a putative tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. In vitro studies have shown menin is localized to the nucleus, possesses two functional nuclear localization signals, and inhibits transcriptional activation by JunD, however, the function of this protein is not known. Two messages have been detected on northern blots but the larger message has not been characterized. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2008],

  • Function:

    disease:Defects in MEN1 are the cause of familial isolated hyperparathyroidism (FIHP) [MIM:145000]; also known as hyperparathyroidism type 1 (HRPT1). FIHP is an autosomal dominant disorder characterized by hypercalcemia, elevated parathyroid hormone (PTH) levels, and uniglandular or multiglandular parathyroid tumors.,disease:Defects in MEN1 are the cause of familial multiple endocrine neoplasia type I (MEN1) [MIM:131100]; an autosomal dominant disorder characterized by tumors of the parathyroid glands, gastro-intestinal endocrine tissue, the anterior pituitary and other tissues. Cutaneous lesions and nervous-tissue tumors can exist. Prognosis in MEN1 patients is related to hormonal hypersecretion by tumors, such as hypergastrinemia causing severe peptic ulcer disease (Zollinger-Ellison syndrome, ZES), primary hyperparathyroidism, and acute forms of hyperinsulinemia.,function:May be invol

  • Subcellular Location:

    Nucleus . Concentrated in nuclear body-like structures. Relocates to the nuclear matrix upon gamma irradiation.

  • Expression:

    Ubiquitous.

  • Western Blot analysis of HuvEc cells using Menin Polyclonal Antibody diluted at 1:500

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Catalog Number

  • Amount:100ul
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Menin Polyclonal Antibody | EnoGene Biotech Co. Ltd