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Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD) Peptid

HPGD Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC

Produktnummer ABIN936298

382,12 €

Zzgl. Versandkosten 20,00 € und MwSt

100 μg

Lieferung nach: Deutschland

Lieferung in 20 bis 27 Werktagen

Kurzübersicht für Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD) Peptid (ABIN936298)

Target

HPGD (Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD))

Spezies

Säugetier

Quelle

Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)

Protein-Typ

Synthetic

Sequenz

DQQQLRDTFR KVVDHFGRLD ILVNNAGVNN EKNWEKTLQI NLVSVISGTY

Produktmerkmale

A synthetic peptide for use as a blocking control in assays to test for specificity of HPGD antibody,
Alternative Names: HPGD control peptide, HPGD antibody Blocking Peptide, Anti-HPGD Blocking Peptide, hydroxyprostaglandin dehydrogenase 15-(NAD Blocking Peptide, Blocking Peptide, PGDH Blocking Peptide, PGDH1 Blocking Peptide, SDR36C1 Blocking Peptide

Aufreinigung

Immunoaffinity purification
Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD) peptide
HPGD Wirt: Synthetic BP, Imm

Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD) (C-Term) peptide
HPGD Reaktivität: Human Wirt: Synthetic BP, BI

Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD) (N-Term) peptide
HPGD Reaktivität: Human Wirt: Synthetic BP, WB

Applikationshinweise

Optimal conditions should be determined by the investigator

Beschränkungen

Nur für Forschungszwecke einsetzbar
Format

Lyophilized

Rekonstitution

Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

Buffer

PBS

Handhabung

Avoid repeated freeze/thaw cycles.

Lagerung

-20 °C

Informationen zur Lagerung

Store at -20 °C long term.
Target

HPGD (Hydroxyprostaglandin Dehydrogenase 15-(NAD) (HPGD))

Hintergrund

This gene encodes a member of the short-chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins, which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht

29 kDa

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