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UROD antibody (AA 1-367)

This anti-UROD antibody is a Rabbit Polyclonal antibody detecting UROD in WB. Suitable for Human.
Catalog No. ABIN6149977

Quick Overview for UROD antibody (AA 1-367) (ABIN6149977)

Target

See all UROD Antibodies
UROD (Uroporphyrinogen Decarboxylase (UROD))

Reactivity

  • 36
  • 10
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
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  • 1
  • 1
Human

Host

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Rabbit

Clonality

  • 36
  • 4
Polyclonal

Conjugate

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  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
This UROD antibody is un-conjugated

Application

  • 34
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  • 9
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  • 4
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Western Blotting (WB)
  • Binding Specificity

    • 15
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    AA 1-367

    Sequence

    MEANGLGPQG FPELKNDTFL RAAWGEETDY TPVWCMRQAG RYLPEFRETR AAQDFFSTCR SPEACCELTL QPLRRFPLDA AIIFSDILVV PQALGMEVTM VPGKGPSFPE PLREEQDLER LRDPEVVASE LGYVFQAITL TRQRLAGRVP LIGFAGAPWT LMTYMVEGGG SSTMAQAKRW LYQRPQASHQ LLRILTDALV PYLVGQVVAG AQALQLFESH AGHLGPQLFN KFALPYIRDV AKQVKARLRE AGLAPVPMII FAKDGHFALE ELAQAGYEVV GLDWTVAPKK ARECVGKTVT LQGNLDPCAL YASEEEIGQL VKQMLDDFGP HRYIANLGHG LYPDMDPEHV GAFVDAVHKH SRLLRQN

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-367 of human UROD (NP_000365.3).

    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

    UROD (Uroporphyrinogen Decarboxylase (UROD))

    Alternative Name

    UROD

    Background

    This gene encodes an enzyme in the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria.,UROD,PCT,UPD,Cell Biology & Developmental Biology,Cardiovascular,Blood,UROD

    Molecular Weight

    40 kDa

    Gene ID

    7389

    UniProt

    P06132
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