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200μL $ 410.00
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For research use only.

Verified Samples Verified Samples in WB: Mouse brain, Mouse cortex, Mouse thymus, Rat brain, Rat cortex, Rat thymus
Dilution WB 1:500-1:2000
Isotype IgG
Host Rabbit
Reactivity Mouse,  Rat
Applications WB
Clonality Polyclonal
Immunogen Recombinant protein corresponding to Mouse CD90
Abbre THY1
Synonyms CD7,  CD90,  CD90 antigen,  CDw90,  FLJ33325,  MGC128895,  T,  T25,  THY1,  Theta antigen,  Thy 1,  Thy 1 T cell antigen,  Thy 1 cell surface antigen,  Thy 1 membrane glycoprotein,  Thy 1.2,  Thy-1 antigen,  Thy-1 membrane glycoprotein,  Thy1,  Thy1 T cell antigen,  Thy1 antigen,  Thy1.1,  Thy1.2
Swissprot
Calculated MW 18 kDa
Observed MW 35-37 kDa
The actual band is not consistent with the expectation.

Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include:

1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein.

2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes.

3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1.

4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids).

5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers.

If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.

Cellular Localization Cell membrane, Membrane.
Concentration 320 μg/mL
Buffer PBS with 0.02% sodium azide, 1% protective protein and 50% glycerol, pH7.4
Purification Method Affinity purification
Research Areas Cancer,  Immunology,  Neuroscience,  Stem Cells
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background Thy-1 or CD90 (Cluster of Differentiation 90) is a 25–37 kDa heavily N-glycosylated, glycophosphatidylinositol(GPI) anchored conserved cell surface protein with a single V-like immunoglobulin domain, originally discovered as a thymocyte antigen.Thy-1 can be used as a marker for a variety of stem cells and for the axonal processes of mature neurons.Structural study of Thy-1 lead to the foundation of the Immunoglobulin superfamily, of which it is the smallest member, and led to some of the initial biochemical description and characterization of a vertebrate GPI anchor and also the first demonstration of tissue specific differential glycosylation.
Cat.No. Product Name Sizes
E-AB-1003 Goat Anti-Rabbit IgG(H+L)(peroxidase/HRP conjugated) 500μL , 120μL , 60μL
E-AB-1043 Streptavidin(peroxidase/HRP conjugated) 500μL , 120μL , 60μL
E-AB-1194 HRP-Goat Anti-Rabbit IgG(H+L) preadsorbed 500μL , 120μL , 1mL
E-IR-R304A Western Blot Detection Kit 50Assays
E-IR-R304B High Accuracy and Absorbability Western Blot Detection Kit 50Assays
Other Clones

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Unconjugated

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