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Immunogen sequence: LHLRNELRDM RAQLGINEDH SEGDEKSEKE TIMAHQPTDV ESTLLQLQEQ NTAIREELNQ LKNENRMLKD RLNALGFSLE QRLDNSEKLF GYQSLSPEIT PGNQSDGGGT LTSSVEGSAP GSVEDLLSQD ENTLMDHQHS NSMDNLDSEC SEVYQPLTSS DDALDAPSSS ESEGIPSIER SRKGSSGNAS EVSVACLTER IHQMEENQHS TSEELQATLQ ELADLQQITQ ELNSENERLG EEKVILMESL CQQSDKLEHF SRQIEYFRSL LDEHHISYVI DEDVKSGRYM ELEQRYMDLA E; Positive Samples: LO2, HeLa, A375; Cellular Location: Cell junction, Cytoplasm, cytoskeleton, gap junction, spindle
This gene encodes a protein that is leucine-rich and is thought to play a role in regulating the interaction of the cytoskeleton with a variety of cellular processes. Mutations in this gene are associated with the French-Canadian type of Leigh syndrome. Transcripts ranging in size from 4. 8 to 7. 0 kb which result from alternative polyadenylation have been reported for this gene.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: cytokinesis and spindle organization A; Cytospin-A; Renal carcinoma antigen NY-REN-22; SPECC1-like; SPECC1-like protein; Sperm antigen with calponin homology and coiled-coil domains 1-like
基因别名: CYTSA; GBBB2; KIAA0376; OBLFC1; SPECC1L
UniProt ID: (Human) B7Z758
Entrez Gene ID: (Human) 23384