IHC/IF accessory reagents

Descrizione Azione

HSP70, a member of the heat shock protein family, is associated with cell division, apoptosis, and tumorigenesis. Studies have found that the expression of HSP70 may be related to the occurrence, development and prognosis of tumors. HSP70 antibodies also directly inhibit apoptosis and have been shown to be involved in the protective effects against heat stress and cytotoxic drugs. HSP70 is upregulated in HCC and is often used in HCC studies together with Glypican-3.

Codice: PA7169_3ml Confezionamento: 3ml
Dettagli

HSP70, a member of the heat shock protein family, is associated with cell division, apoptosis, and tumorigenesis. Studies have found that the expression of HSP70 may be related to the occurrence, development and prognosis of tumors. HSP70 antibodies also directly inhibit apoptosis and have been shown to be involved in the protective effects against heat stress and cytotoxic drugs. HSP70 is upregulated in HCC and is often used in HCC studies together with Glypican-3.

Codice: PA7169_6mL Confezionamento: 6mL
Dettagli

HSP70, a member of the heat shock protein family, is associated with cell division, apoptosis, and tumorigenesis. Studies have found that the expression of HSP70 may be related to the occurrence, development and prognosis of tumors. HSP70 antibodies also directly inhibit apoptosis and have been shown to be involved in the protective effects against heat stress and cytotoxic drugs. HSP70 is upregulated in HCC and is often used in HCC studies together with Glypican-3.

Codice: PA7169_1.5ml Confezionamento: 1.5ml
Dettagli

The IDH1 gene is located at 2q33 and encodes isocitrate dehydrogenase 1. Heterozygous point mutations at codon 132 of IDH1 frequently occur in WHO grade Ⅱ and Ⅲ gliomas. IDH1 gene mutation is somatic cell specific and only occurs in some subtypes of gliomas, which can be used as a basis for glioma subtyping. Heterozygous IDH1 mutation at position 132 occurs in more than 80% of low-grade gliomas, including astrocytoma, oligodendroglioma, oligodendroastrocytoma and secondary glioblastomas. Further studies have shown that the prognosis of IDH1 mutation is significantly better than that of wild type. Therefore, the identification of IDH1 gene mutation is an important reference index for pathological diagnosis and prognosis evaluation.

Codice: PA7185_1.5ml Confezionamento: 1.5ml
Dettagli

The IDH1 gene is located at 2q33 and encodes isocitrate dehydrogenase 1. Heterozygous point mutations at codon 132 of IDH1 frequently occur in WHO grade Ⅱ and Ⅲ gliomas. IDH1 gene mutation is somatic cell specific and only occurs in some subtypes of gliomas, which can be used as a basis for glioma subtyping. Heterozygous IDH1 mutation at position 132 occurs in more than 80% of low-grade gliomas, including astrocytoma, oligodendroglioma, oligodendroastrocytoma and secondary glioblastomas. Further studies have shown that the prognosis of IDH1 mutation is significantly better than that of wild type. Therefore, the identification of IDH1 gene mutation is an important reference index for pathological diagnosis and prognosis evaluation.

Codice: PA7185_6mL Confezionamento: 6mL
Dettagli

The IDH1 gene is located at 2q33 and encodes isocitrate dehydrogenase 1. Heterozygous point mutations at codon 132 of IDH1 frequently occur in WHO grade Ⅱ and Ⅲ gliomas. IDH1 gene mutation is somatic cell specific and only occurs in some subtypes of gliomas, which can be used as a basis for glioma subtyping. Heterozygous IDH1 mutation at position 132 occurs in more than 80% of low-grade gliomas, including astrocytoma, oligodendroglioma, oligodendroastrocytoma and secondary glioblastomas. Further studies have shown that the prognosis of IDH1 mutation is significantly better than that of wild type. Therefore, the identification of IDH1 gene mutation is an important reference index for pathological diagnosis and prognosis evaluation.

Codice: PA7185_3ml Confezionamento: 3ml
Dettagli

The IDH1 gene is located at 2q33 and encodes isocitrate dehydrogenase 1. Heterozygous point mutations at codon 132 of IDH1 frequently occur in WHO grade Ⅱ and Ⅲ gliomas. IDH1 gene mutation is somatic cell specific and only occurs in some subtypes of gliomas, which can be used as a basis for glioma subtyping. Heterozygous IDH1 mutation at position 132 occurs in more than 80% of low-grade gliomas, including astrocytoma, oligodendroglioma, oligodendroastrocytoma and secondary glioblastomas. Further studies have shown that the prognosis of IDH1 mutation is significantly better than that of wild type. Therefore, the identification of IDH1 gene mutation is an important reference index for pathological diagnosis and prognosis evaluation.

Codice: ELAB6945-R_0.2ml Confezionamento: 0.2ml
Dettagli

The IDH1 gene is located at 2q33 and encodes isocitrate dehydrogenase 1. Heterozygous point mutations at codon 132 of IDH1 frequently occur in WHO grade Ⅱ and Ⅲ gliomas. IDH1 gene mutation is somatic cell specific and only occurs in some subtypes of gliomas, which can be used as a basis for glioma subtyping. Heterozygous IDH1 mutation at position 132 occurs in more than 80% of low-grade gliomas, including astrocytoma, oligodendroglioma, oligodendroastrocytoma and secondary glioblastomas. Further studies have shown that the prognosis of IDH1 mutation is significantly better than that of wild type. Therefore, the identification of IDH1 gene mutation is an important reference index for pathological diagnosis and prognosis evaluation.

Codice: ELAB6945-R_0.1ml Confezionamento: 0.1ml
Dettagli

The IDH1 gene is located at 2q33 and encodes isocitrate dehydrogenase 1. Heterozygous point mutations at codon 132 of IDH1 frequently occur in WHO grade Ⅱ and Ⅲ gliomas. IDH1 gene mutation is somatic cell specific and only occurs in some subtypes of gliomas, which can be used as a basis for glioma subtyping. Heterozygous IDH1 mutation at position 132 occurs in more than 80% of low-grade gliomas, including astrocytoma, oligodendroglioma, oligodendroastrocytoma and secondary glioblastomas. Further studies have shown that the prognosis of IDH1 mutation is significantly better than that of wild type. Therefore, the identification of IDH1 gene mutation is an important reference index for pathological diagnosis and prognosis evaluation.

Codice: ELAB6945-R_1mL Confezionamento: 1mL
Dettagli

Immunoglobulin A (IgA) reacts with the A-chain of immunoglobulin IgA, an antibody that plays a key role in mucosal immune function. It has a certain auxiliary significance in the differential diagnosis of plasmacytoma and lymphoplasmacytic lymphoma, and can also be used for the functional classification of glomerulonephritis.

Codice: ELAB6964-R_0.2ml Confezionamento: 0.2ml
Dettagli

Immunoglobulin A (IgA) reacts with the A-chain of immunoglobulin IgA, an antibody that plays a key role in mucosal immune function. It has a certain auxiliary significance in the differential diagnosis of plasmacytoma and lymphoplasmacytic lymphoma, and can also be used for the functional classification of glomerulonephritis.

Codice: ELAB6964-R_0.1ml Confezionamento: 0.1ml
Dettagli

Immunoglobulin A (IgA) reacts with the A-chain of immunoglobulin IgA, an antibody that plays a key role in mucosal immune function. It has a certain auxiliary significance in the differential diagnosis of plasmacytoma and lymphoplasmacytic lymphoma, and can also be used for the functional classification of glomerulonephritis.

Codice: ELAB6964-R_1mL Confezionamento: 1mL
Dettagli