BRP44 anticorps (AA 21-100) (Biotin)
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- Antigène Voir toutes BRP44 Anticorps
- BRP44 (Brain Protein 44 (BRP44))
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Épitope
- AA 21-100
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp BRP44 est conjugé à/à la Biotin
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Application
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Homologie
- Human,Mouse,Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human BRP44
- Isotype
- IgG
- Top Product
- Discover our top product BRP44 Anticorps primaire
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- Indications d'application
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IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- Stockage commentaire
- Store at -20°C for 12 months.
- Date de péremption
- 12 months
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- Antigène
- BRP44 (Brain Protein 44 (BRP44))
- Autre désignation
- BRP44 (BRP44 Produits)
- Synonymes
- anticorps BRP44, anticorps 0610006C01Rik, anticorps 2010002I07Rik, anticorps 2610205H19Rik, anticorps AA108335, anticorps Brp44, anticorps ESTM43, anticorps brp44, anticorps wu:fb22b02, anticorps wu:fb22g07, anticorps zgc:56391, anticorps zgc:86614, anticorps MGC53394, anticorps DKFZp459F1815, anticorps RGD1563422, anticorps mitochondrial pyruvate carrier 2, anticorps mitochondrial pyruvate carrier 2 S homeolog, anticorps uncharacterized protein, anticorps MPC2, anticorps Mpc2, anticorps mpc2, anticorps mpc2.S, anticorps LOC706595, anticorps LOC100285678
- Sujet
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Synonyms: ESTM43, MGC125753, BR44_HUMAN, Brain protein 44, BRP44, DKFZp564B167, MGC125752, rCG_46381, RGD1563422, RP1-295C6.1.
Background: BRP44 is a 127 amino acid protein belonging to the UPF0041 family. The gene that encodes BRP44 maps to human chromosome 1, which is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
- ID gène
- 25874
- Pathways
- L'effet Warburg
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