NIPAL3 anticorps (AA 1-100) (Biotin)
-
- Antigène Tous les produits NIPAL3
- NIPAL3 (NIPA-Like Domain Containing 3 (NIPAL3))
-
Épitope
- AA 1-100
-
Reactivité
- Humain
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp NIPAL3 est conjugé à/à la Biotin
-
Application
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Réactivité croisée
- Humain
- Homologie
- Mouse,Rat,Cow,Sheep,Pig,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human NIPAL3
- Isotype
- IgG
-
-
- Indications d'application
-
WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
-
- 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
-
- Antigène
- NIPAL3 (NIPA-Like Domain Containing 3 (NIPAL3))
- Autre désignation
- NIPAL3 (NIPAL3 Produits)
- Synonymes
- anticorps DJ462O23.2, anticorps NPAL3, anticorps 9130020G22Rik, anticorps AI480660, anticorps Npal3, anticorps RGD1563439, anticorps NIPA like domain containing 3, anticorps NIPA-like domain containing 3, anticorps NIPAL3, anticorps Nipal3
- Sujet
-
Synonyms: NPAL3, NPAL-3, NIPA like domain containing 3, NIPA like protein 3, RGD1563439, RP23-332E2.5, RP3-462O23.3, NPAL3_HUMAN.
Background: NIPAL3 is a 406 amino acid multi-pass membrane protein that belongs to the NIPA family and exists as three alternatively spliced isoforms. The gene that encodes NPAL3 consists of approximately 57,229 bases and maps to human chromosome 1p36. Chromosome 1 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 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.
-