DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19) Antibody
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
Description
DNAJC19 Antibody is a Rabbit Polyclonal against DNAJC19.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19) |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Recommended Dilution | WB: 1/1000 - 1/5000, IHC: 1/20 - 1/200, IP: 1/200 - 1/2000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Antigen Affinity Chromatography. |
| Size 1 | 20 µl |
| Size 2 | 50 µl |
| Size 3 | 100 µl |
| Size 4 | 200 µl |
| Size 5 | 1 ml |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC, IP |
| Buffer | PBS, pH 7.3, containing 0.02% sodium azide and 50% glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q96DA6 |
| Gene ID | 131118 |
| NCBI Accession | NP_001177162.1, NM_001190233.1, NP_660304.1, NM_145261.3 |
| OMIM | 608977 |
| Background | Antibody anti-DNAJC19 |
| Status | RUO |
Descripción
Related Products
DNAJC19 antibody
The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19.
Ver Producto
Recombinant Human DNAJC19
Ver Producto
DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19) Antibody
DNAJC19 Antibody is a Rabbit Polyclonal antibody against DNAJC19. The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19.
Ver Producto