Descrizione Azione

VRL1 Antibody detects endogenous levels of total VRL1.

Codice: DF13915 Confezionamento: 200ul
Dettagli

It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The LOC147645 gene product has been provisionally designated LOC147645 pending further characterization.

Codice: E-AB-17553_20μL Confezionamento: 20μL
Dettagli

It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The LOC147645 gene product has been provisionally designated LOC147645 pending further characterization.

Codice: E-AB-17553_200μL Confezionamento: 200μL
Dettagli

It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The LOC147645 gene product has been provisionally designated LOC147645 pending further characterization.

Codice: E-AB-17553_60μL Confezionamento: 60μL
Dettagli

It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The LOC147645 gene product has been provisionally designated LOC147645 pending further characterization.

Codice: E-AB-17553_120μL Confezionamento: 120μL
Dettagli

VSIG2 Antibody detects endogenous levels of total VSIG2.

Codice: DF2446 Confezionamento: 200ul
Dettagli

VSIG2 Antibody detects endogenous levels of total VSIG2.

Codice: DF2446 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human VSIG2, corresponding to a region within the internal amino acids.

Codice: BF8452 Confezionamento: 200ul
Dettagli

A synthesized peptide derived from human VSIG2, corresponding to a region within the internal amino acids.

Codice: BF8452 Confezionamento: 100ul
Dettagli

VSIG4 Antibody detects endogenous levels of VSIG4.

Codice: DF14591 Confezionamento: 100ul
Dettagli

VSIG4 Antibody detects endogenous levels of VSIG4.

Codice: DF14591 Confezionamento: 200ul
Dettagli

VSIG4 Mouse Monoclonal Antibody detects endogenous levels of VSIG4.

Codice: BF8698 Confezionamento: 200ul
Dettagli