C19orf47 anticorps
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- Antigène Tous les produits C19orf47
- C19orf47 (Chromosome 19 Open Reading Frame 47 (C19orf47))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C19orf47 est non-conjugé
- Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C19orf47
- Isotype
- IgG
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- C19orf47 (Chromosome 19 Open Reading Frame 47 (C19orf47))
- Autre désignation
- C19orf47 (C19orf47 Produits)
- Synonymes
- anticorps MGC79696, anticorps chromosome 19 open reading frame 47, anticorps chromosome 19 open reading frame 47 L homeolog, anticorps RIKEN cDNA 2310022A10 gene, anticorps similar to CG16812-PA, anticorps chromosome 18 open reading frame, human C19orf47, anticorps C19orf47, anticorps c19orf47.L, anticorps c19orf47, anticorps 2310022A10Rik, anticorps RGD1307554, anticorps C18H19orf47
- Sujet
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Synonyms: Uncharacterized protein C19orf47, Chromosome 19 open reading frame 47, DKFZp686P05129, FLJ36888, Hypothetical protein LOC126526, CS047_HUMAN.
Background: C19orf47 is a 422 amino acid protein that exists as three alternatively spliced isoforms and are encoded by a gene located on human chromosome 19. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. 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.
- ID gène
- 126526
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