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  • PHGDH Antibodies

OriGene

PHGDH Monoclonal Antibody (OTI5C4), TrueMAB™

View all (33) PHGDH antibodies

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Cite PHGDH Monoclonal Antibody (OTI5C4), TrueMAB™

  • Antibody Testing Data (3)
PHGDH Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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PHGDH Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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PHGDH Antibody (CF806763) in IHC (P)

Immunohistochemical staining of paraffin-embedded human liver tissue within the normal limits using anti-PHGDH mouse monoclonal antibody. (Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120°C for 3min, TA806763) {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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PHGDH Antibody in Immunohistochemistry (Paraffin) (IHC (P))
PHGDH Antibody in Western Blot (WB)
PHGDH Antibody in Western Blot (WB)
PHGDH Monoclonal Antibody (OTI5C4), TrueMAB™

Product Details

CF806763

Applications
Tested Dilution
Publications

Western Blot (WB)

1:2,000
-

Immunohistochemistry (Paraffin) (IHC (P))

1:150
-
Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG2a

Class

Monoclonal

Type

Antibody

Clone

OTI5C4

Immunogen

Full length human recombinant protein of human PHGDH produced in HEK293T cell.
View immunogen

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Lyophilized

Concentration

1 mg/mL

Purification

Affinity chromatography

Storage buffer

PBS, pH 7.3, with 8% trehalose

Contains

no preservative

Storage conditions

-20°C, Avoid Freeze/Thaw Cycles

Shipping conditions

Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, we recommend adding 100 µL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiments, we strongly recommend performing another round of desalting. (Zeba Spin Desalting Columns, 7KMWCO, 0.5 mL, Product # 89882)

Target Information

PHGDH 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.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: 2-oxoglutarate reductase; 3-PGDH; 3-phosphoglycerate dehydrogenase; D-3-phosphoglycerate dehydrogenase; epididymis secretory protein Li 113; Malate dehydrogenase

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Gene Aliases: 3-PGDH; 3PGDH; HEL-S-113; NLS; NLS1; PDG; PGAD; PGD; PGDH; PGDH3; PHGDH; PHGDHD; SERA

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UniProt ID: (Human) O43175

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Entrez Gene ID: (Human) 26227

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Function(s)
phosphoglycerate dehydrogenase activity electron carrier activity NAD binding
Process(es)
glutamine metabolic process glycine metabolic process L-serine biosynthetic process threonine metabolic process brain development serine family amino acid biosynthetic process gamma-aminobutyric acid metabolic process regulation of gene expression taurine metabolic process spinal cord development glial cell development neural tube development neuron projection development oxidation-reduction process G1 to G0 transition
It has to be done as per old AB suggested Products section.
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If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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