Analytical Data
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基因名
VPS33A
- Application
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别名
VPS33AVacuolar Protein sorting-associated Protein 33A; hVPS33A
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种属
Human
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表达系统
E. coli
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标签
His tag N-Terminus
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
Q96AX1
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表达区间
1-596 aa
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氨基酸序列
MAAHLSYGRV NLNVLREAVR RELREFLDKC AGSKAIVWDE YLTGPFGLIA QYSLLKEHEV EKMFTLKGNR LPAADVKNII FFVRPRLELM DIIAENVLSE DRRGPTRDFH ILFVPRRSLL CEQRLKDLGV LGSFIHREEY SLDLIPFDGD LLSMESEGAF KECYLEGDQT SLYHAAKGLM TLQALYGTIP QIFGKGECAR QVANMMIRMK REFTGSQNSI FPVFDNLLLL DRNVDLLTPL ATQLTYEGLI DEIYGIQNSY VKLPPEKFAP KKQGDGGKDL PTEAKKLQLN SAEELYAEIR DKNFNAVGSV LSKKAKIISA AFEERHNAKT VGEIKQFVSQ LPHMQAARGS LANHTSIAEL IKDVTTSEDF FDKLTVEQEF MSGIDTDKVN NYIEDCIAQK HSLIKVLRLV CLQSVCNSGL KQKVLDYYKR EILQTYGYEH ILTLHNLEKA GLLKPQTGGR NNYPTIRKTL RLWMDDVNEQ NPTDISYVYS GYAPLSVRLA QLLSRPGWRS IEEVLRILPG PHFEERQPLP TGLQKKRQPG ENRVTLIFFL GGVTFAEIAA LRFLSQLEDG GTEYVIATTK LMNGTSWIEA LMEKPF
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分子量
67.6 kDa
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内毒素
< 1.0 EU per μg protein as determined by the LAL method.
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性状
Freeze-dried powder
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缓冲液
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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复溶方法
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- 个性化定制
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稳定性测试
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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保存条件 & 期限
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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运输条件
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
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Protein Description
The VPS33A protein plays a crucial role in the regulation of intracellular trafficking and membrane dynamics, particularly in the context of vesicle transport and fusion processes. This protein is a member of the VPS (vacuolar protein sorting) family, which is known for its involvement in transporting proteins to lysosomes and other membrane-bound organelles. Mutations or deficiencies in VPS33A have been linked to various genetic disorders, including Schimke immuno-osseous dysplasia, which is characterized by immunodeficiency, skeletal abnormalities, and growth retardation. Consequently, studying VPS33A and its associated pathways is essential for understanding the fundamental mechanisms of cellular transport and potential therapeutic targets for related diseases. Additionally, the characterization of VPS33A as a recombinant protein has gained interest in the scientific community, as it enables further investigation into its structure-function relationship and interactions with other cellular components. Investigating VPS33A's biochemical properties, interaction networks, and role in disease mechanisms can provide insights into the development of novel therapeutic strategies for lysosomal storage disorders and other conditions linked to vesicular transport dysfunction. Overall, the study of VPS33A serves as a critical platform for advancing our knowledge of cellular processes and their implications in human health.
