SHMT1 anticorps (N-Term)

N° du produit ABIN5537530

Cet anticorps anti-SHMT1 est un anticorps Lapin Polyclonal détectant SHMT1 dans WB et IHC (p). Adapté pour Humain.

Aperçu rapide pour SHMT1 anticorps (N-Term) (ABIN5537530)

Antigène: SHMT1 (serine Hydroxymethyltransferase 1 (Soluble) (SHMT1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SHMT1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-SHMT1 anticorps

Épitope: AA 19-47, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This SHMT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 19-47 amino acids from the N-terminal region of human SHMT1.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur SHMT1

Antigène: SHMT1 (serine Hydroxymethyltransferase 1 (Soluble) (SHMT1))

Autre désignation: SHMT1

Sujet: This gene encodes the cellular form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing of this gene results in 2 transcript variants encoding 2 different isoforms. Additional transcript variants have been described, but their biological validity has not been determined.

Poids moléculaire: 53 kDa

ID gène: 6470

UniProt: P34896