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ITEM#: 3042-MAB397A4
MFR#: MAB397A4
Anti-GluR2 Antibody, clone 6C4, Alexa Fluor(R) 488 Conjugate clone 6C4, from mouse, ALEXA FLUOR(R) 488
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
Anti-Lamin A/C Antibody, clone 2E8.2 Antibody, Alexa Fluor(R) 488 Conjugate clone 2E8.2, from mouse, ALEXA FLUOR(R) 488
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Lamin-A/C (UniProt: P02545; also known as 70 kDa lamin, Renal carcinoma antigen NY-REN-32) is encoded by the LMNA (also known as LMN1) gene (gene ID: 4000) in human. Lamins are components of the nuclear lamina, a fibrous layer on the nucleoplasmic si | 3042-MABT538AF488 | EA | |
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Anti-N-cadherin Antibody, CT Antibody, clone 6A9.2 Antibody, Alexa Fluor(R) 488 Conjugate clone 6A9.2, from mouse, ALEXA FLUOR(R) 488
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Cadherin-2 (UniProt P19022; also known as CD325, CDw325, N-cadherin, Neural cadherin) is encoded by the CDH2 (also known as CDHN, NCAD) gene (Gene ID 1000) in human. N-Cadherin is a single-pass type I membrane protein that plays a role in calcium-dep | 3042-MABT530AF488 | EA | |
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Anti-Connexin 43 Antibody, CT Antibody, clone 1C5.1 Antibody, Alexa Fluor(R) 488 Conjugate clone 1C5.1, from mouse, ALEXA FLUOR(R) 488
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Gap junction alpha-1 protein (UniProt: P17302; also known as Connexin-43, Cx43, Gap junction 43 kDa heart protein) is encoded by the GJA1 (also known as GJAL) gene (gene ID: 2697) in human. Cx43 is a member of the connexin family of proteins and a co | 3042-MABT528AF488 | EA | |
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Anti-GAPDH Antibody, clone 6C5, Alexa Fluor(R) 488 conjugate clone 6C5, from mouse, ALEXA FLUOR(R) 488
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Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) is an ubiquitous glycolytic enzyme present in reasonably high levels in almost all tissues. The complete and functional enzyme is a tetramer with each of four identical subunits occupying the vertex of | 3042-MAB374AF488 | EA | |
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Anti-C9ORF72/C9RANT (poly-GA) Antibody, clone 5E9 Antibody, Alexa Fluor(R) 488 Conjugate clone 5E9, from mouse, ALEXA FLUOR(R) 488
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Expansion of a GGGGCC hexanucleotide repeat sequence in the non-coding region of human chromosome 9 open reading frame 72 or C9orf72 (also known as ALSFTD, FTDALS; Gene ID 203228) is the most common genetic abnormality in familial and sporadic fronto | 3042-MABN889AF488 | EA |