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HFE antibody (AA 80-306)

This anti-HFE antibody is a Rabbit Polyclonal antibody detecting HFE in WB. Suitable for Human.
Catalog No. ABIN3021896

Quick Overview for HFE antibody (AA 80-306) (ABIN3021896)

Target

See all HFE Antibodies
HFE (Hemochromatosis (HFE))

Reactivity

  • 53
  • 9
  • 7
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 49
  • 6
Rabbit

Clonality

  • 49
  • 6
Polyclonal

Conjugate

  • 27
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  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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  • 1
This HFE antibody is un-conjugated

Application

  • 43
  • 20
  • 15
  • 13
  • 13
  • 5
  • 5
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 16
    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 80-306

    Sequence

    SSQMWLQLSQ SLKGWDHMFT VDFWTIMENH NHSKESHTLQ VILGCEMQED NSTEGYWKYG YDGQDHLEFC PDTLDWRAAE PRAWPTKLEW ERHKIRARQN RAYLERDCPA QLQQLLELGR GVLDQQVPPL VKVTHHVTSS VTTLRCRALN YYPQNITMKW LKDKQPMDAK EFEPKDVLPN GDGTYQGWIT LAVPPGEEQR YTCQVEHPGL DQPLIVIWEP SPSGTLV

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 80-306 of human HFE (NP_000401.1).

    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.

    Handling Advice

    Avoid freeze / thaw cycles

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    HFE (Hemochromatosis (HFE))

    Alternative Name

    HFE

    Background

    The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined.,HFE,HFE1,HH,HLA-H,MVCD7,TFQTL2,Signal Transduction,Endocrine & Metabolism,Neuroscience,Neurodegenerative Diseases Markers,Other Neurological disorders,Stem Cells,Hematopoietic Progenitors,Amyotrophic lateral sclerosis-ALS,HFE

    Molecular Weight

    8 kDa/18 kDa/27-40 kDa

    Gene ID

    3077

    UniProt

    Q30201

    Pathways

    Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process
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