Descrizione Azione

A synthesized peptide derived from human RHAG.

RHAG Antibody
Codice: DF14587 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human RHAG.

RHAG Mouse Monoclonal Antibody
Codice: BF8659 Confezionamento: 100ul
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-19025_200μL Confezionamento: 200μL
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-19025_120μL Confezionamento: 120μL
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-19025_20μL Confezionamento: 20μL
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-19025_60μL Confezionamento: 60μL
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-52939_60μL Confezionamento: 60μL
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-52939_120μL Confezionamento: 120μL
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-52939_200μL Confezionamento: 200μL
Dettagli

The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.

RHAG Polyclonal Antibody
Codice: E-AB-52939_20μL Confezionamento: 20μL
Dettagli

A synthesized peptide derived from human RHBDD1.

RHBDD1 Antibody
Codice: DF14975 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from Human RHBDD2.

RHBDD2 Antibody
Codice: DF14219 Confezionamento: 100ul
Dettagli
1…15935159361593715938159391594015941…19199

Da oltre 35 anni supportiamo la Ricerca e la Diagnostica di Laboratorio

TEMA RICERCA

Link utili

Contatti

Telefono

Tel: 051 62 40 700 – Fax: 051 62 40 706

Email

info@temaricerca.com
P.IVA 00674091202

Indirizzo

Via XXI Ottobre 1944, 11/2 – 40055 Castenaso (BO)

2025 TEMA Ricerca - All Rights Reserved.