Recombinant Full Length Human AFAP1L2 Protein, GST-tagged
Cat.No. : | AFAP1L2-1009HF |
Product Overview : | Human AFAP1L2 full-length ORF ( NP_001001936.1, 1 a.a. - 818 a.a.) recombinant protein with GST-tag at N-terminal. |
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Description : | AFAP1L2 (Actin Filament Associated Protein 1 Like 2) is a Protein Coding gene. Among its related pathways are Cytoskeletal Signaling. GO annotations related to this gene include SH3 domain binding and protein tyrosine kinase activator activity. An important paralog of this gene is AFAP1. |
Source : | In Vitro Cell Free System |
Species : | Human |
Tag : | GST |
Molecular Mass : | 117.7 kDa |
Protein Length : | 818 amino acids |
AA Sequence : | MERYKALEQL LTELDDFLKI LDQENLSSTA LVKKSCLAEL LRLYTKSSSS DEEYIYMNKV TINKQQNAES QGKAPEEQGL LPNGEPSQHS SAPQKSLPDL PPPKMIPERK QLAIPKTESP EGYYEEAEPY DTSLNEDGEA VSSSYESYDE EDGSKGKSAP YQWPSPEAGI ELMRDARICA FLWRKKWLGQ WAKQLCVIKD NRLLCYKSSK DHSPQLDVNL LGSSVIHKEK QVRKKEHKLK ITPMNADVIV LGLQSKDQAE QWLRVIQEVS GLPSEGASEG NQYTPDAQRF NCQKPDIAEK YLSASEYGSS VDGHPEVPET KDVKKKCSAG LKLSNLMNLG RKKSTSLEPV ERSLETSSYL NVLVNSQWKS RWCSVRDNHL HFYQDRNRSK VAQQPLSLVG CEVVPDPSPD HLYSFRILHK GEELAKLEAK SSEEMGHWLG LLLSESGSKT DPEEFTYDYV DADRVSCIVS AAKNSLLLMQ RKFSEPNTYI DGLPSQDRQE ELYDDVDLSE LTAAVEPTEE ATPVADDPNE RESDRVYLDL TPVKSFLHGP SSAQAQASSP TLSCLDNATE ALPADSGPGP TPDEPCIKCP ENLGEQQLES LEPEDPSLRI TTVKIQTEQQ RISFPPSCPD AVVATPPGAS PPVKDRLRVT SAEIKLGKNR TEAEVKRYTE EKERLEKKKE EIRGHLAQLR KEKRELKETL LKCTDKEVLA SLEQKLKEID EECRGEESRR VDLELSIMEV KDNLKKAEAG PVTLGTTVDT THLENVSPRP KAVTPASAPD CTPVNSATTL KNRPLSVVVT GKGTVLQKAK EWEKKGAS |
Applications : | Enzyme-linked Immunoabsorbent Assay Western Blot (Recombinant protein) Antibody Production Protein Array |
Storage : | Store at -80 centigrade. Aliquot to avoid repeated freezing and thawing. |
Storage Buffer : | 50 mM Tris-HCl, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. |
Gene Name : | AFAP1L2 actin filament associated protein 1-like 2 [ Homo sapiens ] |
Official Symbol : | AFAP1L2 |
Synonyms : | AFAP1L2; actin filament associated protein 1-like 2; XB130; KIAA1914 |
Gene ID : | 84632 |
mRNA Refseq : | NM_032550.2 |
Protein Refseq : | NP_115939.1 |
MIM : | 612420 |
UniProt ID : | Q8N4X5 |
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (10)
Ask a questionDysregulation or dysfunction of AFAP1L2 protein can disrupt cellular homeostasis, perturb molecular signaling networks, and contribute to disease progression.
Various experimental techniques or assays, such as immunoprecipitation, live-cell imaging, or functional assays, have been used to study the functional significance of AFAP1L2 protein.
Genetic variations or mutations in the gene encoding AFAP1L2 protein may impact its expression or function, influencing cellular processes or disease susceptibility.
Post-translational modifications and regulatory mechanisms modulate the activity or stability of AFAP1L2 protein.
AFAP1L2 protein interacts with specific molecules or forms protein complexes, which have functional implications in cellular processes.
AFAP1L2 protein plays a role in cellular processes such as actin cytoskeleton dynamics, cell migration, or cell adhesion, and its function can be investigated using techniques like siRNA knockdown or overexpression studies.
The subcellular localization of AFAP1L2 protein can be experimentally determined using techniques such as immunofluorescence microscopy or subcellular fractionation.
AFAP1L2 protein holds potential as a target for modulating cellular processes, and further research is needed to explore its therapeutic implications and potential interventions.
The expression of AFAP1L2 protein is regulated by specific factors and signaling pathways.
AFAP1L2 protein contributes to disease development or pathophysiological conditions, and the underlying molecular mechanisms are currently being investigated.
Customer Reviews (3)
Write a reviewProbing protein-protein interactions in DNA damage response for genome stability.
Deciphering protein-protein interactions in intracellular trafficking for cellular transport.
Elucidating protein-protein interactions in cytoskeletal dynamics for cell motility.
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