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MSQC4

Sigma-Aldrich

SILuLite SigmaMAb 通用抗体标准品 人

同義詞:

IgG1 光, 人 SILuLite SigmaMAb 通用抗体标准品, SigmaMAb

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About This Item

分類程式碼代碼:
23201100
NACRES:
NA.12

重組細胞

expressed in CHO cells

品質等級

運輸包裝

wet ice

儲存溫度

−20°C

相關類別

一般說明

SILU Lite SigmaMAb 是一种重组人单克隆 IgG1λ 轻抗体,在 CHO 细胞中表达的分子量约为 150 kDa。其旨在优化单克隆抗体、生物仿制药和药品的准确完整质量分析。对这种大型生物分子进行准确的完整质量分析可以提供有关结构和翻译后修饰(如糖基化)的全面信息。其他信息如异质性、批间变异、氨基酸截断以及 N-末端 Lys 加工、聚集和降解等均可确定。在治疗性单克隆抗体药物开发中,使用质谱法进行完整质量分析对于配制和储存也非常重要。
该产品由两条相同的重链和两条相同的轻链组成。重链和轻链通过一个二硫键连接。重链通过位于铰链区的两个二硫键连接。其他 12 个半胱氨酸键在分子内仅限于 6 个不同的球状结构域。采用 4 种不同的酶:糜蛋白酶、Asp-N 和 Glu-C 内切蛋白酶和胰蛋白酶,通过完整质量和肽图谱分析评价抗体序列。获得了 100% 的序列覆盖率。

應用

以 SILu Lite SigmaMAb 通用抗体标准人为模型系统,研究气相单克隆抗体 (mAb) 解折叠与 mAb 糖基化离散水平之间的定量关系。

特點和優勢

SigmaMAb 轻链、重链和完整蛋白(糖型丰度最高)的分子量计算值如下:

描述/组成/更改/平均质量 (Da)

还原轻链/C1006H1555N267O333S7 / 焦谷氨酸 (Q) / 22942.2

还原重链/C2181H3393N587O663S16 / (无更改)/ 48957.8
C2237H3485N591O702S16 / G0F / 50403.2
C2243H3495N591O707S16 / G1F / 50565.3
C2249H3505N591O712S16 / G2F / 50727.5

天然完整质量,非还原型 / C6374H9864N1708O1992S46 / 2 X 焦谷氨酸 (Q) / 143767.7
C6486H10048N1716O2070S46 / G0F+G0F / 146658.4
C6492H10058N1716O2075S46 / G0F+G1F / 146820.6
C6498H10068N1716O2080S46 / G1F+G1F / 146982.7
C6504H10078N1716O2085S46 / G1F+G2F / 147144.8
C6510H10088N1716O2090S46 / G2F+G2F / 147307.0

外觀

以含有磷酸盐缓冲盐水的冻干粉形式提供

準備報告

当使用磷酸盐缓冲液 (pH 值为 6-7) 复溶冻干品时,SigmaMAb 回收率最大。

分析報告

SigmaMab 重链
EVQLVESGGGLVQPGGSLRLSCVASGFTLNNYDMHWVRQGIGKGLEWVSKI
GTAGDRYYAGSVKGRFTISRENAKDSLYLQMNSLRVGDAAVYYCARGAGRW
APLGAFDIWGQGTMVTVSS|ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYF
PEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVN
HKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISR
TPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRV
VSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPS
RDELTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFL
YSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPG

SigmaMab 轻链
QSALTQPRSVSGSPGQSVTISCTGTSSDIGGYNFVSWYQQHPGKAPKLMIY
DATKRPSGVPDRFSGSKSGNTASLTISGLQAEDEADYYCCSYAGDYTPGV
VFGGGTKLTVL|GQPKAAPSVTLFPPSSEELQANKATLVCLISDFYPGAVTV
AWKADSSPVKAGVETTTPSKQSNNKYAASSYLSLTPEQWKSHRSYSCQ
VTHEGSTVEKTVAPTECS
也可作为稳定同位素标记产品,Silu Mab(产品编号 MSQC3)
根据 A280 测定的蛋白含量确定包装规格

其他說明

避免使用 PBS 进行复溶。
通过加入 500 μL 超纯水或磷酸盐缓冲液复溶小瓶内容物,并剧烈混匀。溶解后的产物可根据需要进一步稀释。

法律資訊

SILu is a trademark of Sigma-Aldrich Co. LLC

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Yutong Jin et al.
mAbs, 11(1), 106-115 (2018-09-20)
The pharmaceutical industry's interest in monoclonal antibodies (mAbs) and their derivatives has spurred rapid growth in the commercial and clinical pipeline of these effective therapeutics. The complex micro-heterogeneity of mAbs requires in-depth structural characterization for critical quality attribute assessment and
"Collision Induced Unfolding Detects Subtle Differences in Intact Antibody Glycoforms and Associated Fragments.
Tian Y and Brandon T R
International Journal of Mass Spectrometry (2017)
Daniel A Polasky et al.
Analytical chemistry, 91(4), 3147-3155 (2019-01-23)
Ion mobility-mass spectrometry (IM-MS) has become an important addition to the structural biology toolbox, but separating closely related protein conformations remain challenging. Collision-induced unfolding (CIU) has emerged as a valuable technique for distinguishing iso-cross-sectional protein and protein complex ions through
Jared B Shaw et al.
Analytical chemistry, 90(18), 10819-10827 (2018-08-18)
Compared to traditional collision induced dissociation methods, electron capture dissociation (ECD) provides more comprehensive characterization of large peptides and proteins as well as preserves labile post-translational modifications. However, ECD experiments are generally restricted to the high magnetic fields of FTICR-MS
Xi Qiu et al.
Bioanalysis, 10(13), 1055-1067 (2018-07-05)
Sample extraction using immuno-affinity capture coupled with LC-high-resolution mass spectrometer has recently emerged as a novel approach for the determination of concentrations of large molecules at intact level in biological matrix. In the current work, different data processing strategies for

文章

Residual presence of host cell proteins (HCPs) in recombinant therapeutic products has considerable clinical safety risks associated with a potential immunological response in patients.

The use of PNGase Fast denaturing buffer and enzyme yielded results similar to a conventional 20-hour protocol with overnight digest while reducing workflow time to about 1 hour with a 15-minute digest.

條款

SigmaMab Antibody Drug Conjugate Mimic, is a non-toxic drug mimic utilized as a standard for mass spectrometry and high performance liquid chromatography.

Antibody Drug Conjugate Mimic Enables LC-MS Method Development Without Risk

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