钙非依赖性磷脂酶A2(iPLA2)重组蛋白
  • 钙非依赖性磷脂酶A2(iPLA2)重组蛋白

钙非依赖性磷脂酶A2(iPLA2)重组蛋白

Recombinant Phospholipase A2, Calcium Independent (iPLA2)
钙非依赖性磷脂酶A2(iPLA2)重组蛋白应用:SDS-PAGE; WB。
价格 3020
规格: 50µg/200µg/500µg/1mg/5mg
货号: IC811Hu

钙非依赖性磷脂酶A2(iPLA2)重组蛋白

Recombinant Phospholipase A2, Calcium Independent (iPLA2)

PLA2G6; CaI-PLA2; GVI; INAD1; PNPLA9; Ca2+ Independent PLA2; 85 kDa Calcium-Independent Phospholipase A2; Phospholipase A2,group VI(Cytosolic,Calcium-Independent)

[ PROPERTIES ]

Source: Prokaryotic expression. Host: E. coli

Residues: Arg484~Ile701

Tags: N-terminal His-Tag

Tissue Specificity: Testis, Lung, Liver, Kidney. Subcellular Location: Cytoplasm. Purity: >98%

Traits: Freeze-dried powder

Buffer formulation: 100mM NaHCO3, 500mM NaCl, pH8.3, containing 1mM

EDTA, 1mM DTT, 0.01% sarcosyl, 5%Trehalose and Proclin300. Original Concentration: 200µg/mL

Applications: Positive Control; Immunogen; SDS-PAGE; WB. (May be suitable for use in other assays to be determined by the end user.)

Predicted isoelectric point: 9.4

Predicted Molecular Mass: 32.0kDa

Accurate Molecular Mass: 29kDa as determined by SDS-PAGE reducing conditions. Phenomenon explanation:

The possible reasons that the actual band size differs from the predicted are as

follows:

1. Splice variants: Alternative splicing may create different sized proteins from the same gene. 2. Relative charge: The composition of amino acids may affects the charge of the protein. 3. Post-translational modification: Phosphorylation, glycosylation, methylation etc. 4. Post-translation cleavage: Many proteins are synthesized as pro-proteins, and then cleaved to

give the active form. 5. Polymerization of the target protein: Dimerization, multimerization etc.

 [ USAGE ]

Reconstitute in 100mM NaHCO3, 500mM NaCl (pH8.3) to a concentration of0.1-1.0 mg/mL. Do not vortex.

[ STORAGE AND STABILITY ]

Storage: Avoid repeated freeze/thaw cycles. Store at 2-8

oC for one month. Aliquot and store at -80

oC for 12 months. 

Stability Test: The thermal stability is described by the loss rate. The loss ratewas determined by accelerated thermal degradation test, that is, incubate theprotein at 37oC for 48h, and no obvious degradation and precipitation wereobserved. The loss rate is less than 5% within the expiration date under

appropriate storage condition.

[ SEQUENCE ]


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