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Rabbit Anti-Tubulin alpha/Gold Conjugated antibody (bs-20496R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-20496R-Gold
英文名稱 Rabbit Anti-Tubulin alpha/Gold Conjugated antibody
中文名稱 膠體金標記的微管蛋白α 1A/1B抗體
別    名 TUBA1A + TUBA1B; Tubulin, Alpha 1b; Tubulin Alpha-Ubiquitous Chain; Alpha-Tubulin Ubiquitous; Tubulin K-Alpha-1; Tubulin, Alpha, Ubiquitous; Tubulin Alpha-1B Chain; Alpha Tubulin; Ubiquitous; K-ALPHA-1; Tubulin Alpha; TBA1B_HUMAN; Tubulin, Alpha 1a; TUBA3; Tubulin Alpha-3 Chain; Tubulin B-Alpha-1; LIS3; Tubulin, Alpha, Brain-Specific; Tubulin Alpha-1A Chain; Alpha-Tubulin 3, Brain-Specific; Hum-A-Tub1; Hum-A-Tub2; B-ALPHA-1; TBA1A_HUMAN;   
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
產品類型 內參抗體 
研究領域 細胞生物  免疫學  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, Rat,  (predicted: Human, Chicken, Pig, Cow, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 50kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TUBA1A + TUBA1B
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 background:
Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulins. The genes encoding these microtubule constituents belong to the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes, which are highly conserved among species. This gene encodes alpha tubulin and is highly similar to the mouse and rat Tuba1 genes. Northern blotting studies have shown that the gene expression is predominantly found in morphologically differentiated neurologic cells. This gene is one of three alpha-tubulin genes in a cluster on chromosome 12q. Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly, mental retardation, and early-onset epilepsy and caused by defective neuronal migration. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012]

Function:
Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain

Subunit:
Dimer of alpha and beta chains. A typical microtubule is a hollow water-filled tube with an outer diameter of 25 nm and an inner diameter of 15 nM. Alpha-beta heterodimers associate head-to-tail to form protofilaments running lengthwise along the microtubule wall with the beta-tubulin subunit facing the microtubule plus end conferring a structural polarity. Microtubules usually have 13 protofilaments but different protofilament numbers can be found in some organisms and specialized cells.

Subcellular Location:
Cytoplasm, cytoskeleton.

Tissue Specificity:
Ubiquitously expressed with highest levels in Brain, Bone, Adipocyte, and Breast

Post-translational modifications:
Undergoes a tyrosination/detyrosination cycle, the cyclic removal and re-addition of a C-terminal tyrosine residue by the enzymes tubulin tyrosine carboxypeptidase (TTCP) and tubulin tyrosine ligase (TTL), respectively.
Some glutamate residues at the C-terminus are polyglutamylated. This modification occurs exclusively on glutamate residues and results in polyglutamate chains on the gamma-carboxyl group. Also monoglycylated but not polyglycylated due to the absence of functional TTLL10 in human. Monoglycylation is mainly limited to tubulin incorporated into axonemes (cilia and flagella) whereas glutamylation is prevalent in neuronal cells, centrioles, axonemes, and the mitotic spindle. Both modifications can coexist on the same protein on adjacent residues, and lowering glycylation levels increases polyglutamylation, and reciprocally. The precise function of such modifications is still unclear but they regulate the assembly and dynamics of axonemal microtubules (Probable).
Acetylation of alpha chains at Lys-40 stabilizes microtubules and affects affinity and processivity of microtubule motors. This modification has a role in multiple cellular functions, ranging from cell motility, cell cycle progression or cell differentiation to intracellular trafficking and signaling (By similarity).

Similarity:
Belongs to the tubulin family.

Database links:

TUBA1A:

Entrez Gene: 7846 Human

Entrez Gene: 22142 Mouse

Entrez Gene: 64158 Rat

Omim: 602529 Human

SwissProt: Q71U36 Human

SwissProt: P68369 Mouse

SwissProt: P68370 Rat

Unigene: 654422 Human

Unigene: 405359 Mouse

Unigene: 234326 Rat


TUBA1B:

Entrez Gene: 10376 Human

Entrez Gene: 22143 Mouse

Entrez Gene: 500929 Rat

Omim: 602530 Human

SwissProt: P68363 Human

SwissProt: P05213 Mouse

SwissProt: Q6P9V9 Rat

Unigene: 524390 Human

Unigene: 392113 Mouse

Unigene: 99661 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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