Note: Application as IHC, only suitable for histochemical staining or fluorescence staining of paraffin-embedded sections. Application as ICC/IF, suitable for histochemical or fluorescent staining of frozen sections, as well as chemical and fluorescent staining at the cellular level.
注意:抗体应用为IHC的,抗体只适合于石蜡切片的组化染色或者荧光染色。
抗体应用为IF/ICC的,抗体适合于冰冻切片的组化染色或者荧光染色,以及细胞水平的化学染色和荧光染色。
ABMART实验方案下载
SNX32 is a 403 amino acid protein that contains one PX (phox homology) domain and belongs to the sorting nexin family. Existing as two alternatively spliced isoforms, SNX32 may be involved in several stages of intracellular trafficking. The gene that encodes SNX32 consists of approximately 23,256 bases and maps to human chromosome 11q13.1. Housing over 1,400 genes and comprising nearly 4% of the human genome, chromosome 11 is considered a gene and disease association-dense chromosome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that map to chromosome 11. In addition, the blood disorders Sickle cell anemia and thalassemia are caused by mutations in the HBB gene, which is located on chromosome 11.
Sorting nexin-32 (Sorting nexin-6B) SNX32 SNX6B
Human
WB,IHC
WB 1:1000-3000IHC 1:50-200
31/46kDa
254122
q86xe0
A synthetic peptide of human SNX32(150-200/403aa)
Rabbit
Polyclonal Antibody
IgG
Cytoplasm
Protein transport
Affinity purification
Buffer: PBS with 50% Glycerol, 0.03% Proclin300, 0.5% BSA, pH 7.3.
Store at -20℃. Avoid freeze / thaw cycles.
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