|Tested species reactivity||Human, Mouse|
|Published species reactivity||Rabbit, Human, Not Applicable|
|Host / Isotype||Mouse / IgG3|
|Immunogen||Human SSEA4 antigen|
|Storage buffer||PBS, pH 7.4|
|Contains||0.1% sodium azide|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||Assay Dependent|
|Immunocytochemistry (ICC)||Assay Dependent|
|Immunofluorescence (IF)||Assay Dependent|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
FUT4 may catalyze alpha-1,3 glycosidic linkages involved in the expression of Lewis X/SSEA-1 and VIM-2 antigens.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Differential Characterization of Two Kinds of Stem Cells Isolated from Rabbit Nucleus Pulposus and Annulus Fibrosus.
41-4000 was used in immunocytochemistry identify and characterize stem cells in the nucleus pulposus and annulus fibrosus
|Sang C,Cao X,Chen F,Yang X,Zhang Y||Stem cells international (2016:null)||2016|
Harmful Effects of Leukocyte-Rich Platelet-Rich Plasma on Rabbit Tendon Stem Cells In Vitro.
41-4000 was used in immunocytochemistry to study rabbit tendon stem cells in vitro by harmful effects of leukocyte-rich platelet-rich plasma
|Zhang L,Chen S,Chang P,Bao N,Yang C,Ti Y,Zhou L,Zhao J||The American journal of sports medicine (44:1941)||2016|
|Not Applicable||Not Cited||
X-Chromosome Inactivation Analysis in Different Cell Types and Induced Pluripotent Stem Cells Elucidates the Disease Mechanism in a Rare Case of Mucopolysaccharidosis Type II in a Female.
41-4000 was used in immunocytochemistry to elucidate the mechanism responsible for a rare case of a female with mucopolysaccharidosis type II via X-chromosome inactivation analysis in different cell types and induced pluripotent stem cells
|¿eboun M,Rybová J,Dobrovolný R,V¿elák J,Veselková T,¿torkánová G,Mu¿álková D,H¿ebí¿ek M,Ledvinová J,Magner M,Zeman J,Pe¿ková K,Dvo¿áková L||Folia biologica (62:82)||2016|
Gene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.
41-4000 was used in immunocytochemistry to research human iPS-derived motor neurons from sporadic ALS patients for gene expression and a strong association between neurodegeneration and mitochondrial functions
|Alves CJ,Dariolli R,Jorge FM,Monteiro MR,Maximino JR,Martins RS,Strauss BE,Krieger JE,Callegaro D,Chadi G||Frontiers in cellular neuroscience (9:null)||2015|
Mesenchymal stem cells in rabbit meniscus and bone marrow exhibit a similar feature but a heterogeneous multi-differentiation potential: superiority of meniscus as a cell source for meniscus repair.
41-4000 was used in immunocytochemistry to test if mesenchymal stem cells that reside in meniscus maintain specific traits are better for meniscus regeneration
|Ding Z,Huang H||BMC musculoskeletal disorders (16:null)||2015|
Identification of rabbit annulus fibrosus-derived stem cells.
41-4000 was used in immunocytochemistry to isolate and characterize mesenchymal stem cells from rabbit annulus fibrosus tissue
|Liu C,Guo Q,Li J,Wang S,Wang Y,Li B,Yang H||PloS one (9:null)||2014|
Cord blood Lin(-)CD45(-) embryonic-like stem cells are a heterogeneous population that lack self-renewal capacity.
41-4000 was used in immunocytochemistry to isolate, characterize, and expand embryonic-like stem cells from human umbilical cord blood.
|Alvarez-Gonzalez C,Duggleby R,Vagaska B,Querol S,Gomez SG,Ferretti P,Madrigal A||PloS one (8:null)||2013|
||Applications of quantitative polymerase chain reaction protein assays during reprogramming.||Ruff D,MacArthur C,Tran H,Bergseid J,Tian J,Shannon M,Chen SM,Fontes A,Laurent L,Swartzman E,Taliana A,Rao M,Lieu PT||Stem cells and development (21:530)||2012|
Differential properties of human ACL and MCL stem cells may be responsible for their differential healing capacity.
41-4000 was used in immunocytochemistry to characterize stem cells in human anterior cruciate and medial collateral ligaments.
|Zhang J,Pan T,Im HJ,Fu FH,Wang JH||BMC medicine (9:null)||2011|
Clathrin assembly proteins AP180 and CALM in the embryonic rat brain.
41-4000 was used in immunocytochemistry to investigate the changes of clathrin assembly proteins AP180 and CALM during neuronal development
|Schwartz CM,Cheng A,Mughal MR,Mattson MP,Yao PJ||The Journal of comparative neurology (518:3803)||2010|
Characterization of differential properties of rabbit tendon stem cells and tenocytes.
41-4000 was used in immunocytochemistry to characterize rabbit tendon stem/progenitor cells
|Zhang J,Wang JH||BMC musculoskeletal disorders (11:null)||2010|
|Not Applicable||Not Cited||
Stage-specific embryonic antigens (SSEA-3 and -4) are epitopes of a unique globo-series ganglioside isolated from human teratocarcinoma cells.
41-4000 was used in immunocytochemistry to use MC631 and MC813-70 to study glycolipids in human teratocarcinoma
|Kannagi R,Cochran NA,Ishigami F,Hakomori S,Andrews PW,Knowles BB,Solter D||The EMBO journal (2:2355)||1984|
A study to identify and characterize the stem/progenitor cell in rabbit meniscus.
41-4000 was used in immunocytochemistry to examine the role of meniscus-derived stromal cells in healing
|Huang H,Wang S,Gui J,Shen H||Cytotechnology (68:2083)||2016|
|Not Applicable||Not Cited||
Affinity of monoclonal antibodies for Globo-series glycans.
41-4000 was used to assess the affinity of monoclonal antibodies to the glycans present in SSEA-4 and Globo H
|Eller CH,Yang G,Ouerfelli O,Raines RT||Carbohydrate research (397:1)||2014|
Prostaglandin E2 (PGE2) exerts biphasic effects on human tendon stem cells.
41-4000 was used in immunocytochemistry to determine the biphasic effects of PGE2 on human tendon stem/progenitor cells.
|Zhang J,Wang JH||PloS one (9:null)||2014|
|Human||Not Cited||Cellular characterization of human pluripotent stem cells.||Quintanilla RH||Methods in molecular biology (Clifton, N.J.) (997:179)||2013|
|Human||Not Cited||Applications of quantitative polymerase chain reaction protein assays during reprogramming.||Ruff D,MacArthur C,Tran H,Bergseid J,Tian J,Shannon M,Chen SM,Fontes A,Laurent L,Swartzman E,Taliana A,Rao M,Lieu PT||Stem cells and development (21:530)||2012|