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MCFD2 antibody (AA 27-146)

This anti-MCFD2 antibody is a Rabbit Polyclonal antibody detecting MCFD2 in WB and IHC. Suitable for Human.
Catalog No. ABIN6143636

Quick Overview for MCFD2 antibody (AA 27-146) (ABIN6143636)

Target

See all MCFD2 Antibodies
MCFD2 (Multiple Coagulation Factor Deficiency 2 (MCFD2))

Reactivity

  • 25
  • 23
  • 22
Human

Host

  • 29
  • 11
Rabbit

Clonality

  • 30
  • 10
Polyclonal

Conjugate

  • 9
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MCFD2 antibody is un-conjugated

Application

  • 27
  • 15
  • 13
  • 13
  • 7
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 7
    • 2
    • 1
    AA 27-146

    Sequence

    EEPAASFSQP GSMGLDKNTV HDQEHIMEHL EGVINKPEAE MSPQELQLHY FKMHDYDGNN LLDGLELSTA ITHVHKEEGS EQAPLMSEDE LINIIDGVLR DDDKNNDGYI DYAEFAKSLQ

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 27-146 of human MCFD2 (NP_644808.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:100 - 1:200

    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

    MCFD2 (Multiple Coagulation Factor Deficiency 2 (MCFD2))

    Alternative Name

    MCFD2

    Background

    This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1, also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D), a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms.,MCFD2,F5F8D,F5F8D2,LMAN1IP,SDNSF,Signal Transduction,MCFD2

    Molecular Weight

    10 kDa/14 kDa/16 kDa

    Gene ID

    90411

    UniProt

    Q8NI22
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