Comparison

EMC8 Antibody

Item no. CSB-PA276232-50ul
Manufacturer Cusabio
Amount 50 ul
Quantity options 100 ul 50 ul
Category
Type Antibody Polyclonal
Format Liquid
Applications WB, IHC, ELISA
Specific against Human (Homo sapiens), Mouse (Murine, Mus musculus), Rat (Rattus norvegicus)
Host Rabbit
Isotype IgG
Conjugate/Tag Unconjugated
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias C16orf2 antibody,C16orf4 antibody,COX4 neighbor antibody,COX4,neighbor of antibody,COX4AL antibody,Cox4nb antibody,CX4NB_HUMAN antibody,ER membrane protein complex subunit 8 antibody,FAM158B antibody,family with sequence similarity 158,member B antibody,Neighbor of COX4 antibody,NOC4 antibody,Protein FAM158B antibody
Similar products ER membrane protein complex subunit 8
Available
Manufacturer - Type
Polyclonal Antibody
Manufacturer - Applications
ELISA, WB, IHC; ELISA:1:2000-1:5000, WB:1:500-1:2000, IHC:1:50-1:200
Manufacturer - Targets
EMC8
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Manufacturer - Alias
C16orf2 antibody, C16orf4 antibody, COX4 neighbor antibody, COX4, neighbor of antibody, COX4AL antibody, Cox4nb antibody, CX4NB_HUMAN antibody, ER membrane protein complex subunit 8 antibody, FAM158B antibody, family with sequence similarity 158, member B antibody, Neighbor of COX4 antibody, NOC4 antibody, Protein FAM158B antibody
Immunogen Species
Human
Immunogen
Fusion protein of human EMC8
Dilution
ELISA:1:2000-1:5000
WB:1:500-1:2000
IHC:1:50-1:200
Background
COX4NB (Neighbor of COX4) is a 210 amino acid protein encoded by the human gene COX4NB. COX4NB belongs to the UPF0172 (NOC4) family and is found on chromosome 16, adjacent to the gene that encodes COX4. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other auto-immune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
Buffer
pH7.4 of PBS, 0.05% NaN3, 40% Glycerol.
Purification Method
Antigen Affinity Purified
General Research Areas
Cell Biology
Initial Research Areas
Cell Biology
Antigen Species
Human
Antigen
Fusion protein of Human EMC8
Clonality
Polyclonal

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 50 ul
Available: In stock
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