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100μL $ 230.00
50μL $ 125.00
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For research use only.

Verified Samples Verified Samples in WB: Mouse colon, Mouse skin, Mouse colon, Mouse skin
Dilution WB 1:500-1:1000
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse
Applications WB
Clonality Polyclonal
Immunogen Recombinant Human LMNA protein expressed by E.coli
Abbre LMNA
Synonyms 70 kDa lamin,  CDCD1,  CDDC,  CMD1A,  CMT2B1,  Cardiomyopathy dilated 1A (autosomal dominant),  EMD2,  FPL,  FPLD,  FPLD2,  HGPS,  IDC,  LDP1,  LFP,  LGMD1B,  LMN 1,  LMN A,  Lamin,  Lamin A,  Lamin A/C,  Lamin A/C like 1,  Lamin C,  Lamin-A/C,  Limb girdle muscular dystrophy 1B (autosomal dominant)
Swissprot
Calculated MW 63,64,65,69,71,74 kDa
Observed MW 71 ,74 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.

Concentration 1 mg/mL
Buffer PBS with 0.05% proclin 300, 1% protective protein and 50% glycerol,pH7.4
Purification Method Affinity purification
Research Areas Cancer,  Signal Transduction,  Tags and Cell Markers
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 The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants.
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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