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PHGDH antibody (AA 264-533)

This anti-PHGDH antibody is a Rabbit Polyclonal antibody detecting PHGDH in WB, IF and IP. Suitable for Human.
Catalog No. ABIN6145554

Quick Overview for PHGDH antibody (AA 264-533) (ABIN6145554)

Target

See all PHGDH Antibodies
PHGDH (phosphoglycerate Dehydrogenase (PHGDH))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This PHGDH antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP)
  • Binding Specificity

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    AA 264-533

    Sequence

    EEPPRDRALV DHENVISCPH LGASTKEAQS RCGEEIAVQF VDMVKGKSLT GVVNAQALTS AFSPHTKPWI GLAEALGTLM RAWAGSPKGT IQVITQGTSL KNAGNCLSPA VIVGLLKEAS KQADVNLVNA KLLVKEAGLN VTTSHSPAAP GEQGFGECLL AVALAGAPYQ AVGLVQGTTP VLQGLNGAVF RPEVPLRRDL PLLLFRTQTS DPAMLPTMIG LLAEAGVRLL SYQTSLVSDG ETWHVMGISS LLPSLEAWKQ HVTEAFQFHF

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 264-533 of human PHGDH (NP_006614.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200,IP,1:50 - 1:200

    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

    PHGDH (phosphoglycerate Dehydrogenase (PHGDH))

    Alternative Name

    PHGDH

    Background

    This gene encodes the enzyme which is involved in the early steps of L-serine synthesis in animal cells. L-serine is required for D-serine and other amino acid synthesis. The enzyme requires NAD/NADH as a cofactor and forms homotetramers for activity. Mutations in this gene have been found in a family with congenital microcephaly, psychomotor retardation and other symptoms. Multiple alternatively spliced transcript variants have been found, however the full-length nature of most are not known.,PHGDH,3-PGDH,3PGDH,HEL-S-113,NLS,NLS1,PDG,PGAD,PGD,PGDH,PHGDHD,SERA,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,Neuroscience,PHGDH

    Molecular Weight

    56 kDa

    Gene ID

    26227

    UniProt

    O43175

    Pathways

    Metabolism of Steroid Hormones and Vitamin D, Warburg Effect
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