ARG47439

anti-KBTBD10 / KRP1 antibody

anti-KBTBD10 / KRP1 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Overview

Product Description Mouse Monoclonal antibody recognizes KBTBD10 / KRP1
Tested Reactivity Hu, Ms
Tested Application IHC-P, WB
Host Mouse
Clonality Monoclonal
Isotype IgG2a
Target Name KBTBD10 / KRP1
Antigen Species Human
Immunogen Recombinant protein of Human KBTBD10 / KRP1.
Conjugation Un-conjugated
Alternate Names KLHL41; Kelch-like protein 41; KBTBD10; KRP1; Kel-like protein 23; Kelch repeat and BTB domain-containing protein 10; Kelch-related protein 1; Sarcosin

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P
WB
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purification with Protein A
Buffer PBS, 0.09% Sodium azide, 50% Glycerol and 0.5% BSA
Preservative 0.09% Sodium azide
Stabilizer 50% Glycerol and 0.5% BSA
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 10324 Human KLHL41

GeneID: 228003 Mouse KLHL41

Swiss-port # A2AUC9 Mouse Kelch-like protein 41

Swiss-port # O60662 Human Kelch-like protein 41

Gene Symbol KLHL41
Gene Full Name kelch like family member 41
Background This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]
Function Involved in skeletal muscle development and differentiation. Regulates proliferation and differentiation of myoblasts and plays a role in myofibril assembly by promoting lateral fusion of adjacent thin fibrils into mature, wide myofibrils. Required for pseudopod elongation in transformed cells. [UniProt]
Cellular Localization Cytoplasm; Cytoskeleton; Cell projection; Membrane; Endoplasmic reticulum membrane. [UniProt]
Calculated MW 68 kDa
PTM Phosphoprotein; Ubl conjugation. [UniProt]